1. No category

Corporate Add. – D-204, Budh Nagar, Inder Puri, Loha Mandi,
Naraina, New Delhi- 110012.
Contact us - +91-8586871108, +91-7503606803,+91-8802442463
E-Mail ID - ucskamal@gmail.com.
[ UNITY CONSULTANCY SERVICES]
[UNITY CONSULTANCY SERVICES is a prominent service provider, offering ISO Certification Services,
Export Certificates, Quality Management Services, Engineering Management Services, Total Quality Management,
CE Marking, OHSAS Certification, NABL Certification, SSI/MSME Registration, Factory Pollution Cert etc.]
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UNITY CONSULTANCY
SERVICES
COMPANY PROFILE
The certification plays an important role in building a strong reputation in the international market.
These certifications are mainly provided to those organizations who maintain quality in their work
process, policies and practices. Established in the year 2009, UNITY CONSULTANCY SERVICES is a
prominent service provider, offering ISO Certification Services, Export Certificates, Quality Management
Services, Engineering Management Services, Total Quality Management, CE Marking, OHSAS
Certification etc. Our services are recognized for being customized, effective and completion of projects
within the stipulated time and budget.
Our organization is committed to the continual improvement of our individual processes and ensures
that there is the provision of value added services for our clients. Our team is completely involved in the
work and takes appropriate decisions to execute the assignments in a proper way. We maintain a
cordial relationship with our clients and our vast industrial experience, in-depth knowledge and
transparent business policies has helped us in gaining the faith of our clients. We have been
appreciated by various clients due to our innovative way of providing solutions to clients. Our
consultants with their know how assist our clients on attaining certifications. Moreover, our experts
closely work with our clients and help them to utilize all resources and implement necessary
improvements in their infrastructure facilities that meet the strict quality parameters of various
certifications.
INSPIRED BY QUALITY, COMMITTED TO EXCELLENCE
UNITY CONSULTANCY SERVICES is one of the largest & leading business management consulting
organizations offering business management consulting services to organizations of all nature and size.
We provide one of the most comprehensive suites of consulting services, products & training in the
fields of Quality Management, Marketing Management, Human Resources Management, and Finance
Management & Strategic Management to the organizations across all the industry verticals for building
a progressive and profitable organization by creating a sustainable competitive advantage in the
market.
UNITY CONSULTANCY SERVICES specializes in the entire range of ISO management system
certification standards. Our consultants provide world class consulting services and training for
achieving ISO 9001 Quality Management, ISO 14001 Environment Management, HACCP ISO 22000
Food Safety Management, OHSAS 18001, SA 8000 Social Accountability, ISO 27001 ISMS etc.
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UNITY CONSULTANCY
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UNITY CONSULTANCY
SERVICES
Unity consultancy services is one of the few management system certifications consulting organizations
in the world having domain expertise and project implementation experience across the business
domains and industry verticals.
Our strength is company specific business management consulting / ISO Consulting solutions so that a
small organization of 10 employees can implement any of the ISO standards with equal effectiveness
as compared to a multi Locations, multi products/service organization of 5000 or more employees.
QUALITY ASSURANCE
We, at Unity Consultancy Services, are Committed to Continually Improve its Quality System by :
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Providing Services of Consistent Quality to the Satisfaction of our Customers.
Internal Customer Focus and Beneficial Relationship with Suppliers and Customers.
Continual Improvement on new policies and Quality Management System Based on National &
International Standards.
Involvement of all employees in Improvement and Innovation in all Spheres of Management.
RESEARCH & DEVELOPMENT
We have a research and development unit, which is constantly working in order to make our
consultancy services more streamlined for our valued clients. Our R & D department provides updated
information to our clients in order to maintain their goodwill in line with the market. Our R & D unit takes
care of the following functions:
WHY UNITY CONSULTANCY SERVICES
We have achieved a good amount of success due to the following factors:
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Qualified Team of 50 People
Industry Leading Rates
Advanced Technology
Speedy Solutions
Wide Connectivity
Innovative Ideas
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UNITY CONSULTANCY
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UNITY CONSULTANCY
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Proven track record in designing, deploying, training, auditing and certification assistance to
Organizations for systems based on various international standards. Highly skilled and experienced
pool of consultants in all the domains catered to. Strong domain proficiency in all the sectors served.
We are a team of professional engineers having rich industrial experience, practically involved in
development, implementation and monitoring of various systems and “Total Quality Management’ in
organizations, committed to provide consultancy / training in the field of Quality / Environment
Management Systems, Shop-floor improvement practices and other emerging trends in the industries
for the overall improvement and growth of manufacturing and service sectors.
We are in the field of consultancy for the past two years and provided consultancy to different
organizations in various fields.
By our experience, we can easily pinpoint strengths & weaknesses of your processes & help you to
improve your key performance areas. Our Motto is to satisfy the customer by providing best of our
services.
CONSULTANCY SERVICES FOR ISO SERIES
SYSTEM CERTIFICATION AND PRODUCT CERTIFICATION:
Our expert consultants will assist you at every phase of the project, and will provide the tools you need
for successful implementation and improvement of your system. Our standard methodology covers…
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Gap Analysis
Awareness Training Programs
Documentation Training Programs
Process Documentations
PIM Workshops (Ask today about our unique PIM Tool for Process Mapping)
Manual Preparations
Support in Implementation
INTERNAL AUDITOR Training Programs
Assistance in Internal Audits
Assistance in Management Review
Readiness Review Audits
Assistance during Certification Audits
Since all projects are unique and we don’t believe in one-size-fit-all approach; hence our project
management depends on the size of the client, complexity of the processes, urgency of the client, and
competence of people working for client.
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UNITY CONSULTANCY
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UNITY CONSULTANCY
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COST EFFECTIVE ISO PROJECT MANAGEMENT SERVICES:
If you believe you have the right professionals to document your system and you just need consultants
to steer your project till certification and fill in the gaps that are missing in your existing team, we can
assist you with our cost-effective management system project management services. We will steer the
project and oversee all activities done by your team and review and analyze each document or
procedure produced by your team, conduct necessary trainings to ensure that the management system
is adequately understood in the organization, and conduct readiness reviews before you call your
certification company. We ensure under our scope that you get successful certification.
STRATEGIC STAFFING AND HEAD HUNTING SERVICES
We understand the requirement of both employers and employees and suggest the best-fits. Our strong
database of candidates and ever-increasing demand from employers to provide them competent
employees to manage their management systems standards implementation, training and maintenance.
We provide management representatives, management appointees, fresh quality trainees, quality
control professionals with experience in Q.C. Departments, environmental professionals, TQM
professionals, Six Sigma professionals, Balanced Scorecard professionals, Occupational Health and
Safety Professionals, Safety Officers and Managers, Information Security Management System
Professionals, Information Technology Service Management System Professionals, Laboratory
Management system professionals for material testing and calibration laboratories, etc.
All employees recommended by us goes through various pre-qualification phases to ensure the
credibility of their information and their competence as stated in their resumes. Our success rate so far
is much above the industry standard for strategic staffing…
REACH US:
ADMINISTRATIVE OFFICER
UNITY CONSULTANCY SERVICES
Corporate Add. – Building No. D- 204, BUDH NAGAR, NEAR LOHA MANDI , NARAINA, NEW DELHI-110012.
Contact us - +91-8586871108, +91-7503606803,+91-8802442463,
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UNITY CONSULTANCY
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E-Mail ID -
ucskamal@gmail.com
UNITY CONSULTANCY
SERVICES
CONTENTS
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ISO 9001:2008 CERTIFICATION
ISO 14001:2004 CERTIFICATION
OHSAS 18001:2007 CERTIFICATION
ISO/TS 16949:2009 CERTIFICATION
ISO 22000:2005 CERTIFICATION
HACCP CERTIFICATION
ISO 9001:2008 & HACCP CERTIFICATION
ISO 27001:2005 CERTIFICATION
ISO 13485:2003 CERTIFICATION
ISO 20000 CERTIFICATION
ISO 10002 CERTIFICATION
cGMP CERTIFICATION
SA 8000 & SRM CERTIFICATION
WRAP CERTIFICATION
BRC CERTIFICATION
HALAL CERTIFICATION
Oeko-Tex @ Standard 1000 CERTIFICATION
REACH CERTIFICATION
C-TPAT CERTIFICATION
CE MARK CERTIFICATION
KAIZEN SERVICES
SIX SIGMA SERVICES
GAIN CERTIFICATION
GREEN CERTIFICATION
PRODUCT TESTING SERVICES
TRAINING SERVICES
LISIONING FOR DGS&D
LISIONING FOR NSIC
FACTORY ASSESSMENT SERVICES
LISIONING FOR ISI MARK
LISIONING FOR REGISTRATION
LISIONING FOR FPO & MFPO
ACCREDITATION BOARD FOR CERTIFICATION
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UNITY CONSULTANCY
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UNITY CONSULTANCY
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SCHEMES UNDER UNITY CONSULTANCY SERVICES INDIA
€- ISO 9001:2008 CERTIFICATION
ISO 9001 is a Quality Management
Standard. It applies to all types of
organizations. It doesn't matter what
size they are or what they do. It can
help both product and service oriented
organizations achieve standards of
quality that are recognized and
respected throughout the world.
The ISO 9001:2008 quality certification
is based on the following eight
fundamental
quality
management
principles:
* Customer focus
* Leadership
* Involvement of people
* Process approach
* System approach to management
* Continual improvement
* Factual approach to decision making
* Mutually beneficial supplier
relationships Customer Benefits
The ISO 9000 series of standards have been
developed to enable organizations to have
quality based
management systems. This enables them to
understand their customer's requirements and
improve customer satisfaction, through the
review and improvement of their internal
activities.
The benefits of using the standards are as follows:
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Improved consistency of service and product performance
Higher customer satisfaction levels
Improved customer perception
Improved productivity and efficiency
Cost reductions
Improved communications, morale and job satisfaction
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* Competitive advantage and increased marketing and sales opportunities.
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UNITY CONSULTANCY
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HOW CAN UCS HELP?
UCS consists of full-time trainers and consultants with a unique combination of manufacturing
experience, business and financial expertise, and a "hands-on" approach creates a recipe for our
clients' success.
ISO 9001 CONSULTING
Our Team offers a variety of Consulting Services and Solutions.
UCS understands that each organization or person is unique. Our Solutions are comprehensive and will
be customized to meet your specific needs.
For example, our consultants can take your company through ISO 9001 from start to finish, and in most
cases you have ready for registration in 1 to 3 months.
This comprehensive implementation program is tailored to your individual plans and may include:
 A benchmark visit,
 An overview of the standards,
 Writing and revising documentation,
 On-site or off-site training of personnel,
 Assistance with implementation,
 Liaison with the registrar, reassessments and follow-up evaluations, and consulting during
the registration process.
 Annual Training & Support Contract
 Annual Training & Support Contract and Improvement Programs for ISO certified companies
We help you in maintaining and continually improving your certified QMS / EMS so as align with the
changing needs of the customer and organization.
UNITY CONSULTANCY SERVICES helps you with Align documentation for changes in the
organizational needs and structure:
 Continuous training, on latest topics and techniques with Training of new employees
 We provide Internal Audit in every three months.
 Conducting Management Review Meeting at every six months with proper agenda
 If any Nonconformity occurs then we provide Closure of non-conformity with proper
corrective & preventive action to enhance customer satisfaction.
 Reassessment of the Quality Management System in your organization
 Improve existing documentation & Systems for better outputs and results.
 Customer Audits and closure of corrective actions.
If you have any query please give us the mail on
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ucskamal@gmail.com
UNITY CONSULTANCY
SERVICES
UNITY CONSULTANCY
SERVICES
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ISO 14001:2004 CERTIFICATION
ISO 14001:2004 specifies requirements for an
Environmental Management System to enable an
organization to develop and implement a policy and
objectives which take into account legal requirements
and other requirements to which the organization
subscribes, and information about significant
environmental aspects. It applies to those
environmental aspects that the organization identifies
as those, which it can control, and those which it can
influence. It does not itself state specific
environmental performance criteria.
PURPOSE OF ISO 14001
ISO 14001 is an Environmental Management System (EMS) who's purpose is:
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A management commitment to pollution prevention.
An understanding of the environmental impacts (reducing) of an organization's activities.
A commitment (pollution prevention) to employees, neighbours and customers.
FIVE KEY PHASES
Phase 1: Establishing the environmental goals (policy).
Phase 2: Planning the elements of the EMS.
Phase 3: Implementing the EMS.
Phase 4: Checking for any problems and correcting them.
Phase 5: Evaluating the effectiveness of the EMS and improving it, and launching into a new
cycle of improvement.
BENEFITS OF IMPLEMENTING ISO 14001
Reduce cost of waste management
Savings in consumption of energy and materials
Improved compliance
Overall Costs Reduced
Fewer accidents
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UNITY CONSULTANCY
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UNITY CONSULTANCY
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Competitive advantage
Improved use of resources
Framework for continuous improvement of your environmental performance
Improved corporate image among regulators, customers and the public
ISO 14001 INTERNAL AUDITORs Training
Effective auditing is a highly specialized skill and IQMS trains key personnel from your organization to
be successful INTERNAL AUDITORs. We have training programs that range from 1 to 3 days. All
programs can be customized to meet any unique needs that you may have.
The Training will cover following topics:
The requirements of ISO 14001
Auditing techniques compatible with ISO14000
How to plan, perform and report on an audit
How to take corrective action
Architecture of the ISO 14001 Documentation
Preparation of Checklists
Nonconformity - Major and Minor
Learning Outcomes
Better understanding of the ISO 14001 Requirements
Learn how to Conduct Internal Audits, Audit Process and Cycle
Preparing and Using Checklist
How to Seek Objective Evidence
Hands-on/Practical Experience
INTERNAL AUDITOR Certificate (upon successful completion)
Identify opportunities for improvement
HOW CAN UCS HELP?
UCS consists of full-time trainers and consultants with a unique combination of manufacturing
experience, business and financial expertise, and a "hands-on" approach creates a recipe for our
clients' success.
This comprehensive implementation program is tailored to your individual plans and may include
A benchmark visit,
An overview of the standards,
Writing and revising documentation,
On-site or off-site training of personnel,
Assistance with implementation,
Liaison with the registrar, reassessments and follow-up evaluations, and consulting during the
registration process
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UNITY CONSULTANCY
SERVICES
If you have any query please give us the mail on
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ucskamal@gmail.com
UNITY CONSULTANCY
SERVICES
UNITY CONSULTANCY
SERVICES
OHSAS stands for Occupational
Health and Safety Assessment
Series. OHSAS 18001 is a consensus
standard developed in 1999 by an
independent
group of national standards bodies
and certification bodies (registrars).
OHSAS 18001 is structured the same
way as ISO 14001, the environmental
management system standard, and
has essentially the same elements. It
was specifically developed to be
compatible with ISO 9001, the quality
management system standard, and
ISO 14001 to allow companies to
develop and register integrated
quality,
environmental
and
occupational safety and health
management systems.
OHSAS 18001:2007 CERTIFICATION
BENEFITS OF OHSAS CERTIFICATION
Organizations that have implemented a system to improve the management of health and safety
practices have reported reduced improved employee safety awareness, fewer accidents and reduced
costs. In addition, OHSAS 18001 provides a structure, companies can use to integrate quality,
environmental and safety and health program management for increased management efficiencies.
Many companies find they need to address health and safety elements as they implement ISO 14001
management systems because of the strong interconnection between environmental and safety and
health programs in areas such as emergency planning and risk assessment.
THE ELEMENTS OF OHSAS 18001 AND INCLUDE:
Developing an OHS Policy
Hazard Identification & Risk Assessment
Identifying Legal Requirements
Setting OHS Objectives
Establishing an OHS Management Program
Training Employees
Implementing OHS Control Measures
Emergency Planning
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UNITY CONSULTANCY
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Document and Record Control
Internal Audit Programs
Corrective and Preventative Action
Management Involvement and Management Review
Steps to OHSAS 18000 Certification
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UNITY CONSULTANCY
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UNITY CONSULTANCY
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The process for establishing an OHSAS 18001 management system is essentially the same as the
process used of implementing an ISO 14001 system:
Preliminary review of existing programs and systems
Identification of hazards and applicable laws and regulations
Developing new procedures
Training personnel
Implementing new programs such as internal audit and management review
Seeking certification of the OHS program
HOW CAN WE HELP?
KMS consists of full-time trainers and consultants with industry-diverse experience. While we do use
industry proven approaches and methodologies, we tailor these to fit your organization’s specific needs.
A unique combination of manufacturing experience, business and financial expertise, and a "hands-on"
approach creates a recipe for our clients' success. We not only identify and prioritize opportunities to
add significantly to your bottom line; we develop and help our clients implement a plan for exploiting
those opportunities to achieve financially measurable success.
If you have any query please give us the mail on
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ucskamal@gmail.com
UNITY CONSULTANCY
SERVICES
UNITY CONSULTANCY
SERVICES
The ISO/TS16949 is an international
standard aiming to the development of
a quality management system that
provides for continual improvement,
emphasizing defect prevention and
the reduction of variation and waste in
the supply chain.
ISO/TS 16949:2009
CERTIFICATION
TS16949 applies to the design
/development, production and, when
relevant, installation and servicing of
automotive-related products. It is
based on ISO9001.
The requirements are intended to be
applied throughout the supply chain.
For the first time vehicle assembly
plants will be encouraged to seek
ISO/TS16949 certification.
BENEFITS OF TS 16949 CERTIFICATION
Identify opportunities for improvement
High quality auditing will ensure that your organization is always compliant with the necessary
requirements of TS 16949.
Each participant will receive a seminar manual and a team breakout workbook that includes
case studies.
A guide on "how to" audit TS 16949 elements and the objective evidence required will be taught
and provided for participants.
TS 16949 IMPLEMENTATION PROCESS
Management Commitment and Support.
TS 16949 Audit/Assessment (Gap Analysis).
Development of an Implementation Plan.
Provide Awareness Training to all employees.
Allocate Resources that will be necessary to develop and implement the system
Prepare Quality System Documentation - Tier 1, 2, 3 documents (Quality Manual, Quality
System Procedures, Work Instructions and Quality Records/Forms).
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Determine Training Needs of Employees - Job and Employee Skill Matrix (ie. overview of new
system, internal auditing, problem solving, teamwork, etc...).
Implement the New System.
Conduct Internal Audits.
Take Corrective Actions, if necessary.
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UNITY CONSULTANCY
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UNITY CONSULTANCY
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Re-Audit/Follow-up, if necessary.
Registrar Audit Preparation/Training
Registration Application.
Registration Audit.
Registration Certificate Issued.
Maintain, Improve and Innovate the System.
TS 16949 INTERNAL AUDITOR Training
Auditing is critical to ensure compliance and find out the gaps. It maximizes the benefits of
implementing TS 16949. Effective auditing is a highly specialized skill and KMS trains key personnel
from your organization to be successful INTERNAL AUDITORs.
Training Topics
The requirements of TS 16949
Auditing techniques compatible with TS 16949
How to plan, perform and report on an audit
How to take corrective action
Architecture of the TS 16949 Documentation
Preparation of Checklists
Nonconformities - Major and Minor
Seeking Objective Evidence Through Documentation
HOW CAN UCS HELP?
UCS consists of full-time trainers and consultants with a unique combination of manufacturing
experience, business and financial expertise, and a "hands-on" approach creates a recipe for our
clients' success. TS 16949 Consulting
UCS is a management-consulting firm designed to create value for manufacturers and product
developers.
Our clients include organizations from the industrial and consumer products, service and medical
device sectors. Providing training and hands-on consulting services in the areas of TS 16949.We can
help you achieve lower costs, improved productivity, and improved time-to-market.
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If you have any query please give us the mail on
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ucskamal@gmail.com
UNITY CONSULTANCY
SERVICES
UNITY CONSULTANCY
SERVICES
This International Standard ISO 22000
specifies requirements for a food safety
management system where an organization
in the food chain needs to demonstrate its
ability to control food safety hazards in order
to ensure that food is safe at the time of
human consumption.
ISO 22000:2005
CERTIFICATION
It is applicable to all organizations, regardless
of size, which are involved in any aspect of
the food chain and want to implement
systems that consistently provide safe
products. The means of meeting any
requirements of this International Standard
can be accomplished through the use of
internal and/or external resources. This
International Standard ISO 22000 specifies
requirements to enable an organization.
PROCESS OF ISO 22000:2005 CERTIFICATE
To plan, implement, operate, maintain and update a food safety management system aimed at
providing products that, according to their intended use, are safe for the consumer
To demonstrate compliance with applicable statutory and regulatory food safety requirements
To evaluate and assess customer requirements and demonstrate conformity with those mutually
agreed customer requirements that relate to food safety, in order to enhance customer
satisfaction
To effectively communicate food safety issues to their suppliers, customers and relevant
interested parties in the food chain
To ensure that the organization conforms to its stated food safety policy
To demonstrate such conformity to relevant interested parties and
To seek certification or registration of its food safety management system by an external
organization, or make a self-assessment or self-declaration of conformity to this International
Standard.
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If you have any query please give us the mail on
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ucskamal@gmail.com
UNITY CONSULTANCY
SERVICES
UNITY CONSULTANCY
SERVICES
This International Guideline HACCP made by
philsbery specifies requirements for a food
safety management system where an
organization in the food chain needs to
demonstrate its ability to control food safety
hazards in order to ensure that food is safe at
the time of human consumption.
HACCP CERTIFICATION
It is applicable to all organizations, regardless
of size, which are involved in any aspect of
the food chain and want to implement
systems that consistently provide safe
products. The means of meeting any
requirements of this International Standard
can be accomplished through the use of
internal and/or external resources. This
International Guideline HACCP specifies
requirements to enable an organization.
PROCESS OF HACCP CERTIFICATE
To plan, implement, operate, maintain and update a food safety management system aimed at
providing products that, according to their intended use, are safe for the consumer
To demonstrate compliance with applicable statutory and regulatory food safety requirements
To evaluate and assess customer requirements and demonstrate conformity with those mutually
agreed customer requirements that relate to food safety, in order to enhance customer
satisfaction
To effectively communicate food safety issues to their suppliers, customers and relevant
interested parties in the food chain
To ensure that the organization conforms to its stated food safety policy
To demonstrate such conformity to relevant interested parties and
To seek certification or registration of its food safety management system by an external
organization, or make a self-assessment or self-declaration of conformity to this International
Standard.
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UNITY CONSULTANCY
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If you have any query please give us the mail on
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ucskamal@gmail.com
UNITY CONSULTANCY
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UNITY CONSULTANCY
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ISO 9001:2008 & HACCP
CERTIFICATION
This International Standard ISO 9001:2008 &
The Guideline HACCP made by philsbery
specifies requirements for a food safety with
Quality management system where an
organization in the food chain needs to
demonstrate its ability to control food safety
hazards in order to ensure that food is safe at
the time of human consumption.
It is applicable to all organizations, regardless
of size, which are involved in any aspect of
the food chain and want to implement
systems that consistently provide safe
products. The means of meeting any
requirements of this International Standard
can be accomplished through the use of
internal and/or external resources. This
International Standard ISO 9001:2008 & The
Guideline HACCP specifies requirement to
enable an organization.
To plan, implement, operate,
maintain and update a food safety
management system aimed at
providing products that, according to
their intended use, are safe for the
consumer
To demonstrate compliance with
applicable statutory and regulatory food safety requirements
To evaluate and assess customer requirements and demonstrate conformity with those mutually
agreed customer requirements that relate to food safety, in order to enhance customer
satisfaction
To effectively communicate food safety issues to their suppliers, customers and relevant
interested parties in the food chain
To ensure that the organization conforms to its stated food safety policy
To demonstrate such conformity to relevant interested parties and
To seek certification or registration of its food safety management system by an external
organization, or make a self-assessment or self-declaration of conformity to this International
Standard.
If you have any query please give us the mail on
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ucskamal@gmail.com
UNITY CONSULTANCY
SERVICES
UNITY CONSULTANCY
SERVICES
Information Security Management Systems
Certification (ISO/IEC 27001:2013) covers all
types of organizations (e.g. commercial
enterprises, government agencies, not-for
profit organizations). ISO/IEC 27001:2013
specifies the requirements for establishing,
implementing,
operating,
monitoring,
reviewing, maintaining and improving a
documented
Information
Security
Management System within the context of
the organization's overall business risks. It
specifies requirements for the implementation
of security controls customized to the needs
of individual organizations or parts thereof.
ISO 27001:2013 CERTIFICATION
ISO/IEC 27001:2013 is designed to ensure
the selection of adequate and proportionate
security controls that protect information
assets and give confidence to interested
parties.
ISO/IEC 27001:2005 is intended to be
suitable for several different types of use,
including the following:
Use within organizations to formulate security requirements and objectives.
Use within organizations as a way to ensure that security risks are cost effectively managed
Use within organizations to ensure compliance with laws and regulations
Use within an organization as a process framework for the implementation and management of
controls to ensure that the specific security objectives of an organization are met.
Definition of new information security management processes.
Identification and clarification of existing information security management processes
Use by the management of organizations to determine the status of information security
management activities
Use by the internal and external auditors of organizations to determine the degree of compliance
with the policies, directives and standards adopted by an organization
Use by organizations to provide relevant information about information security policies,
directives, standards and procedures to trading partners and other organizations with whom
they interact for operational or commercial reasons
Implementation of business-enabling information security
Use by organizations to provide relevant information about information security to customers
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UNITY CONSULTANCY
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If you have any query please give us the mail on
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ucskamal@gmail.com
UNITY CONSULTANCY
SERVICES
UNITY CONSULTANCY
SERVICES
ISO 13485:2003 CERTIFICATION
All requirements of ISO 13485:2003 are specific to organizations providing medical devices, regardless
of the type or size of the organization.
If regulatory requirements permit exclusions of design and development controls, this can be used as a
justification for their exclusion from the quality management system. These regulations can provide
alternative arrangements that are to be addressed in the quality management system. It is the
responsibility of the organization to ensure that claims of conformity with ISO 13485:2003 reflect
exclusion of design and development controls.
If any requirement(s) in Clause 7 of ISO 13485:2003 is(are) not applicable due to the nature of the
medical device(s) for which the quality management system is applied, the organization does not need
to include such a requirement(s) in its quality management system.
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The processes required by ISO 13485:2003, which are applicable to the medical device(s), but which
are not performed by the organization, are the responsibility of the organization and are accounted for
the organization's quality management system.
Management system for medical device
manufacturers (ISO 13485:2003) specifies
requirements for a quality management
system where an organization needs to
demonstrate its ability to provide medical
devices and related services that consistently
meet customer requirements and regulatory
requirements applicable to medical devices
and related services.
The primary objective of ISO 13485:2003 is
to facilitate harmonized medical device
regulatory
requirements
for
quality
management systems. As a result, it includes
some particular requirements for medical
devices and excludes some of the
requirements of ISO 9001 that are not
appropriate as regulatory requirements.
Because of these exclusions, organizations
whose quality management systems conform
to this International Standard cannot claim
conformity to ISO 9001 unless their quality
management systems conform to all the
requirements of ISO 9001
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TECH TIPS
13485 emphasize meeting regulatory as well as customer requirements, risk management and
maintaining effective processes.
13485 is in part designed to produce a management system that facilitates compliance to the
requirements of customers and global regulators.
Benefits can be reaped from being both 9001 and 13485 certified, because 9001 focuses on
business aspects not found in 13485 that are good for all businesses.
BENEFITS OF DUAL CERTIFICATION: 13485 & 9001
Medical device manufacturers can benefit from being both 9001 and 13485 certified. While such
manufacturers are not required to have 9001 certification, it can bring further business benefits,
because it focuses on business aspects that are good for all businesses—for example, the emphasis on
customer satisfaction and continuous process improvement that a 13485 management system omits.
Manufactures of medical devices also will need to acquire 9001 certification if they want to branch out to
other industries, as 13485 certification will not be honoured where 9001.
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ISO 20000 CERTIFICATION
ISO 20000 CERTIFICATION, ISO 20000
CONSULTANCY, ISO 20000 CONSULTANT,
ISO 20000 TRAINING, ISO 20000 AUDIT, ISO
20000 GAP ANALYSIS, ISO 20000
CHECKLIST
An ISO 20000 certificate is proof that your IT
organization is customer-focused able to deliver
services which meet defined quality levels making
use of resources in an economical way
As such, the ISO 20000 certificate and the corresponding
logo are increasingly a competitive advantage in the
market:
Many clients even demand ISO 20000 compliance
as a condition for awarding contracts to IT service
providers.
Of course, working along ISO 20000 (and ITIL) principles also offers internal benefits for the IT
organization, because the standard is all about supporting the business side with adequate IT services,
while providing those services as efficiently as possible.
The decision to go for an ISO 20000 certificate sets a specific target for your IT organization and helps
to concentrate minds.
We will be pleased to offer ISO 20000 Certification, ISO 20000 Consultancy, ISO 20000 Consultant,
ISO 20000 Training, ISO 20000 Audit, ISO 20000 Gap Analysis, ISO 20000 Checklist
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ISO 10002:2007 CERTIFICATION
ISO 10001 :2007 customer satisfaction
management system & ISO 10002 – Complaint
handling system
This guidelines draws focus on :
Designing Customer Feedback / complaint
handling system
Interpretation of the feedback parameters /
complaint parameters
Data Analysis of the feedback / complaint
root cause
Continual Improvement projects based on
the feedback / corrective actions
In today’s competitive world the organizations that are proactive in managing their customers go
a long way in establishing themselves as industry leaders. The best way to achieve this
leadership is have an efficient customer satisfaction management system and an effective
customer complaint handling system.
ISO 10001 is the standard for how an organization manages it’s customer satisfaction process
and ISO 10002 talks about how an organization manages it’s complaint handling system.
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cGMP CERTIFICATION
W.H.O.
defines
Good
Manufacturing
Practices (GMP) as "that part of quality
assurance which ensures that products are
consistently produced and controlled to the
quality standards appropriate to their
intended use and as required by the
marketing authorization". GMP covers all
aspects of the manufacturing process:
defined manufacturing process; validated
critical
manufacturing
steps;
suitable
premises, storage, transport; qualified and
trained production and quality control
personnel; adequate laboratory facilities;
approved
written
procedures
and
instructions; records to show all steps of
defined procedures taken; full traceability of a
product through batch processing records
and distribution records; and systems for
recall and investigation of complaints.
The guiding principle of GMP is that quality is built into a product, and not just tested into a finished
product. Therefore, the assurance is that the product not only meets the final specifications, but that it
has been made by the same procedures under the same conditions each and every time it is made.
There are many ways this is controlled - controlling the quality of the facility and its systems, controlling
the quality of the starting materials, controlling the quality of production at all stages, controlling the
quality of the testing of the product, controlling the identity of materials by adequate labelling and
segregation, controlling the quality of materials and product by adequate storage, etc. All of these
controls must follow prescribed, formal, approved procedures, written as protocols, SOPs, or Master
Formulae, describing all the tasks carried out in an entire manufacturing and control process.
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SA 8000 CERTIFICATION
The SA 8000 certification is the Social
Accountability System standard. It is
applicable to companies of any size that wish
to address the social and ethical aspects of
their business. A Social Accountability
System proves to customers that the
company holds adequate provisions for the
protection of workers' rights. Further, it
ensures ethical production of all goods
manufactured by the company.
SA 8000 KEY REQUIREMENTS
Be senior management led.
Be focused on continuous improvement.
Be focused on prevention rather than reaction.
Be supportive of workers’ rights and workers participation.
Be compliant with local laws/codes.
Be proactive in promoting ethical sourcing.
Be systematic in addressing problems-CARs Process.
BENEFITS OF SA 8000 TO MANUFACTURERS AND SUPPLIERS
Marketing advantage – more demand and value for goods from socially.
Responsible manufacturers/suppliers.
Enhancement of company’s productivity.
Compliance to the laws of the land.
Improvement of relationship with the Govt., NGOs, trade unions.
Better image and position in labour market.
BENEFITS OF SA 8000 FOR THE RETAILERS
Cost reduction in monitoring.
Better corporate image.
Increased value for the products.
Trust building with the analysts and investors when evaluated against social performance.
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WRAP CERTIFICATION
The Worldwide Responsible Accredited Production (WRAP) program
is the world’s largest facility certification program mainly focused on
the apparel, footwear and sewn products sectors. Facilities receive a
certification of six months to one year based on compliance with the
12 WRAP Principles.
For more details, kindly download the PDF attached.
http://2.imimg.com/data2/EK/HX/MY-/wrap.pdf
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BRC CERTIFICATION
BRC BRITISH RETAIL CONSORTIUM & IFS
INTERNATIONAL FOOD STANDARD GLOBAL
FOOD STANDARD
BRC Global Standard – Food is being adopted by
food suppliers worldwide and especially those
supplying to British retailers. Certification to the
standard helps manufacturers, brand owners and
retailers fulfill their legal obligations whilst
ultimately safeguarding the consumer. The
standard covers all areas of product safety and
legality and addresses part of the due diligence
requirements of the supplier and the retailer.
BRC/IOP Global Standard - Food Packaging and
Other Packaging Materials provides a common
basis for the certification of companies supplying
packaging for food products to retailers.
The standard is particularly suitable for suppliers
of food packaging materials to UK retailers,
regardless of packaging material type or country
Customers, employees, stockholders and competitorsofdevelop
origin. sustainable respect for an organization
which demonstrates its commitment to food safety and/or packaging regulations.
BENEFITS OF BRC
Operating costs drop as rework reduces, efficiencies increase and non-compliance penalties reduce.
BRC is the most applicable standard for the food industry.
By achieving the BRC standard, the company reassures its customers that their product reaches the
customer through a temperature controlled supply chain in consistently good condition.
As a result, retailers feel more confident in doing business with their suppliers.
The BRC drew up a standard for food and required all suppliers and food producers to comply with this
standard.
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Halal is a Quarnic term that simply means
'permitted' or lawful' Halal when used in
relation to food and other consumables means
permissible for consumption and used by
Muslims based on the Islamic law, which is
the Sharjah.
HALAL CERTIFICATION
It is the responsibility of a Muslim to ensure
that any food consumed or any businesses
performed in their daily lives are clean,
hygienic and not detrimental to either their
health or well-being. Halal promotes
cleanliness in all aspcets of a person. It is the
new bench mark for quality.
Halal trade, refers to the trade of certified
quality products that have met rigorous
internationally
accepted
standards
in
production and hygiene.
BENEFITS OF HALAL CERTIFICATION
Opportunities to tap a global Halal food market of about 2 billion people (Middle east, Asia Pacific, EU,
USA, LATAM, Central Asia). Halal logo is an authoritative, independent and reliable testimony to
support Halal food claims 200% profit of greater market share: No loss of non-Muslim markets/clients
Enhance marketability of product in Muslim countries/markets
Small cost investment relative to multiple growth in revenues
Image boosts in meeting varied customer needs
Improve the food preparation hygienic systematically
Improve the food quality into global standards
CERTIFICATION – RELEVANCE TO YOUR BUSINESS
Halal India Certification is becoming more relevant in today's market mainly because people are more
aware of the Halal concept it is not just about religious related matters but it extends to the products or
services being deemed safe for consumption as well as have health benefits. In today's booming Halal
industry, many businesses are seeking to have their Products (food & non food), Premises, Factories,
Merchandise and Services to be Halal certified.
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TYPES OF HALAL CERTIFICATIONS
Eating Establishment Scheme:
 Issued to restaurants, hawkers, school canteen stalls, snack bars, Halal corners,
confectioneries, bakeries and temporary stalls in bazaars, flea market, trade fairs, etc.
Product Scheme:
 Issued to India-made products
Whole Plant Scheme:

Issued to manufacturers for the entire plant
Food Catering Scheme:

Issued to catering establishments and central kitchen facilities
Poultry Abattoir Scheme:

Issued to poultry abattoirs for their freshly-slaughtered poultry
Storage Facility Scheme:

Issued to stationary/mobile storage facilities and warehouses
Endorsement Scheme:

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Issued to manufacturers, importers and exporters who intend to import\export their Halal
certified products
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To complement the product-related OekoTex® Standard 100, the Oeko-Tex® Standard
1000 is a testing, auditing and certification
system for environmentally friendly production
sites throughout the textile processing chain.
Oeko-Tex® Standard 100, the
Oeko-Tex® Standard 1000
CERTIFICATION
To qualify for certification according to the
Oeko- Tex® Standard 1000, companies must
meet stipulated criteria in terms of their
environmentally
friendly
manufacturing
processes and provide evidence that at least
30% of total production is already certified
under Oeko-Tex® Standard 100.
Oeko-Tex Standard 1000
To complement the product-related Oeko-Tex® Standard 100, the Oeko-Tex® Standard 1000 is a
testing, auditing and certification system for environmentally friendly production sites throughout the
textile processing chain
To qualify for certification according to the Oeko-Tex® Standard 1000, companies must meet stipulated
criteria in terms of their environmentally-friendly manufacturing processes and provide evidence that at
least 30% of total production is already certified under Oeko-Tex® Standard 100.
THE REQUIRED CRITERIA INCLUDE:
Use of environmentally-damaging auxiliaries and dyestuffs prohibited
Compliance with standard values for waste water and exhaust air treatment
Optimisation of energy consumption
Avoidance of noise and dust pollution
Defined measures to ensure safety at the workplace
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Use of child labour prohibited
Introduction of basic elements of an environmental management system
The company is monitored by an independent auditor from one of the member institutes of the "OekoTex® International - Association for the Assessment of Environmentally Friendly Textiles". The
certificate is valid for three years.
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ADVANTAGES
The additional cost of certifying and production process according to Oeko-Tex® Standard 1000 offers
textile and clothing companies the following advantages:
Effective public relations documentation of the objectively stipulated ecological measures in
place at a production site
Increased production efficiency and thus reduced costs
Waste minimisation
Increased acceptance of a company's products on the market
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REACH CERTIFICATION - REGISTRATION, EVALUATION & AUTHORIZATION OF
CHEMICALS CERTIFICATION
REACH Certification - Registration, Evaluation &
Authorization of Chemicals
The new European Union chemical policy, REACH (Registration,
Evaluation and Authorization of Chemicals), is aiming at ensuring a
high level of protection of health and the environment as well as
enhancing innovation of green chemicals.
The Regulation (EC) N°1907/2006 of the European
Parliament and of the Council of 18 December 2006 concerning the
Registration, Evaluation, Authorization and Restriction of chemicals
(REACH) and Directive 2006/121/EC of the European Parliament and
of the Council of 18 December 2006 amending Council Directive
67/548/EEC (relating to the classification, packaging and labelling of
dangerous substances) were published in the Official Journal on 30
December 2006
When REACH comes into force on 1 June 2007, it will replace around 40 existing EU Regulations and
Directives so as to provide a single system to regulate chemicals in a more organized manner.
replaces 40 existing EU Chemical Regulations and Directives aims at ensuring a high level of protection
of health and the environment and at giving industrials, EU manufacturers and importers a sense of
responsibility
most industries are affected by REACH (toy, textile, electrical, cosmetic) industries will have to improve
the communication through its supply chain; suppliers will have to provide information on substances;
information about safety to be communicated to the downstream users and distributors
recommends a single system to regulate chemicals of 1 tonne or more on the European market
(priorities on high volumes and substances of very high concern SVHC) data base of registered
substances managed by the European Chemicals Agency (ECHA, 25 Member States) located in
Helsinki, Finland around 30 000 substances will be registered 500 substances are classified as CMR
(Carcinogens, Mutagens, Reprotoxic) with 140 priority substances
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WHO DOES IT AFFECT ?
REACH obliges manufacturers or importers to register substances on its own, in preparation or in article
they place on the EU market with relevant information with a threshold limit of 1 tonne per annum.
Distributors and downstream users will also be concerned by REACH, as they use substances in the
course of their industrial or professional activities.
What will change with this new system of chemicals management?
Under the present legislation public authorities are required to identify and address possible safety
issues for the chemicals on the market. REACH aims at changing this balance by requiring industry to
take responsibility for assessing the risks of chemicals and for ensuring their safe use. At the same
time, improvements in the efficiency of the system are designed to ensure that there are better
incentives for developing new and safer chemicals and that the requirements are drawn up in such a
way that the competitiveness of EU industry is safeguarded.
Then, industries will be responsible for declaring uses of chemical substances in order to assess the
risks inherent in the use.
The REACH implementation project (RIP) carried out a close collaboration between commission
services and stakeholders, member states and industry. Technical guidance documents are prepared
for industry and authorities to facilitate the implementation of the future REACH regulation. It will help to
understand tasks and fulfil obligations under REACH
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C-TPAT CUSTOMS TRADE PARTNERSHIP AGAINST TERRORISM
CERTIFICATION
C-TPAT (Customs - Trade Protection Against Terrorism) is a voluntary
US government-business initiative to build cooperative relationships
that improve overall international supply chain and U.S. border
security.
C-TPAT (Customs - Trade Protection Against Terrorism) is a voluntary
US government-business initiative to build cooperative relationships
that improve overall international supply chain and U.S. border
security. This initiative was launched to assist the trading community
in the war against
Terrorism based on the below criteria:
Business Partner Requirements (Security Procedures)
Container Security (Seals, Container Inspection etc)
Physical Access Control
Procedural Security
Security Training and Awareness
Physical Security
Information Technology
KMS can perform independent assessment through verification audit and confirm each facility about the
compliance status against C-TPAT requirements.
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CE MARK CERTIFICATION FOR ALL DIRECTIVES
The CE marking is a conformity marking consisting of the letters
"CE", and taking the form as shown here. CE is an abbreviation
for 'Conformity European', French for 'European Conformity'.
The CE marking symbolizes that a product it is
affixed to is in conformity with all relevant essential requirements
of the European technical regulations ("Directives"), and that the
product compliance has been established using the appropriate
conformity
assessment
procedure(s).
The
assessential
requirements are requirements related to product safety, public
health and consumer protection.
CE marking is obligatory for any product covered
by one or more of the European technical regulations requiring
the affixing of the CE marking. Without the CE marking, these
products are not allowed to be placed or to be put into service in
Europe. In this regard, the CE marking sometimes is called a
trade passport, because like carrying a passport when entering a
country, the CE Marking is required for market access.
THE NEED OF CE MARKING
The European CE certification procedure has been mainly set up to:
Harmonize all varying national regulations for consumer and industrial products in European
Member States, so that the Single Market is encouraged
Bring about cost savings for producers;
Enhance the safety of products;
Supply public bodies with a uniform procedure that can be checked.
With the help of the conformity assessment procedures, the authorities can ascertain that the
products that are placed on the market comply with the requirements as stated in the regulations
of the directives. The CE marking is consequently largely for the benefit of the authorities.
However, safe products are also necessary for the end user in the work or consumer
environment.
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WHAT ARE THE BENEFITS OF CE MARKING?
The CE Marking is a kind of trade passport for the European marketplace: it allows the manufacturer to
freely circulate their product throughout the 18 countries of the European Economic Area (EEA).
There is only one set of requirements and procedures to comply with in designing and manufacturing a
product for the entire EEA. Various conflicting national regulations are eliminated. As a result, the
product no longer needs to be adapted to the specific requirements of the different member states of
the EEA.
In addition, it may be considered a benefit that by implementing the requirements, the product will be
safer for the user and this may also reduce damage and liability claims.
The CE Marking is NOT required for the following types of products:
Chemicals
Pharmaceuticals
Cosmetics
Foodstuffs
HOW KMS CAN HELP?
KMS ensures that the products of a company comply to the CE marking and CE certification
regulations.
Our expert CE marking services consist out of
Verifying product documentation
Modifying and testing products to ensure compliance with CE marking regulations
Compiling CE mark Technical construction files
Applying CE marking
Authorized Representation
THE CE MARKING IS REQUIRED ONLY FOR THE FOLLOWING TYPES OF DIRECTIVES
TOYS DIRECTIVE
MACHINERY DIRECTIVE
ELECTRICAL EQUIPMENT DIRECTIVE
LOW VOLTAGE DIRECTIVE
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EMC DIRECTIVE
PERSONAL PROTECTIVE EQUIPMENT DIRECTIVE
PRESSURE EQUIPMENT DIRECTIVE
MEDICAL DEVICES DIRECTIVE
ACTIVE IMPLANTABLE MEDICAL DEVICES DIRECTIVE
IN VITRO DIAGNOSTICS DIRECTIVE
RADIO AND TELECOMMUNICATIONS TERMINAL EQUIPMENT DIRECTIVE
SIMPLE PRESSURE VESSELS DIRECTIVE
GAS APPLIANCES DIRECTIVE
LIFTS DIRECTIVE
RECREATIONAL CRAFT DIRECTIVE
EQUIPMENT AND PROTECTIVE SYSTEMS FOR USE IN EXPLOSIVE ATMOSPHERES
DIRECTIVE
NON-AUTOMATIC WEIGHING INSTRUMENTS DIRECTIVE
CABLE WAYS DIRECTIVE
CONSTRUCTION PRODUCTS DIRECTIVE
EXPLOSIVES FOR CIVIL USE DIRECTIVE
NEW HOT WATER BOILERS DIRECTIVE
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KAIZEN SERVICES
KAIZEN is the Japanese strategy of continuous
Improvement. The KAIZEN business strategy involves every
employee of an organization from top management to the
cleaning crew, to work together to make improvements but
without much financial investments.
KAIZEN is a standard to make continuous improvement by
removing waste from all the systems of a workplace. When the
KAIZEN method starts, it develops the workplace and guides
employee how to carry out a new way of thinking about his/her
job. KAIZEN also involves the training that teaches people to
improve their ability to achieve high quality and to think about their
job in a new way. KAIZEN helps organizations to reach a new and
upper level.
PRINCIPLES OF KAIZEN
It recognizes the entire process and the final results.
It considers only the best way to examine the job.
It ensures that the right process is put into place.
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HOW TO PERFORM KAIZEN ACTIVITIES?
Eliminate conventional and meaning less ideas.
Always think for the best suitable way to perform the task.
If there is any mistake or fault then modify it
Never look for perfection even for only ten percent of target.
Never make excuses. Just initiate it.
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Try to find the main causes.
Use your brain instead of spending money for KAIZEN.
Consider the awareness of five employees instead of considering the knowledge of one person.
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SIX SIGMA CERTIFICATION
Six Sigma is a business management strategy,originally developed
by Motorola, that today enjoys wide-spread application in many
sectors of industry.
The word 'Sigma' is a Greek letter used for a statistical term that
measures how far a given process deviates from
perfection(standard deviation).The higher the sigma number, the
closer to perfection. One Sigma is not very good, six sigma means
only 3.4defects per million.
The Idea behind six sigma is that if you can measure how many
”defects” you have in a process, you can systematically figure out
how to eliminate them and get as close to “zero defects” as
possible.
WHAT IS DMAIC?
DMAIC is a basic component of the Six Sigma methodology- a way to improve work processes by
eliminating defects. The Six Sigma methodology is widely used in many top corporations around the
world. It is normally defined as a set of practices that improve efficiency and eliminate defects.
The Six Sigma system strives to reduce these variations in both business and manufacturing and in
order to do so; these processes must be measured, analyzed, controlled and improved upon. In order
to improve upon these processes, the Six Sigma system requires sustained commitment from an entire
organization - especially from the top echelons to help guide lower rung workers and policies. The
DMAIC methodology includes five steps including; Define, Measure, Analyze, Improve and Control.
SIX STEPS TO LEAN SIX SIGMA IMPLEMENTATION
The following is a brief overview explanation of a Six Steps to Lean Six Sigma deployment and
execution process, recommended for small and mid-sized organizations
Reasons to adopt six sigma
Defined process for problem solving
Proven methodology to solve problems
Consistency with results
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Focus on the "bottom line" which encourages credibility/support from the top of the organization.
In today's dynamic business era, where intense competition and perennial change are the order
of the day, it is imperative for organizations to focus on the quality of their products, systems,
and processes.
Quality is the measure of customer's satisfaction derived from the use of a particular product or
service. Quality is always measured from the customer's perspective. It is the adherence of
organizational processes to the set benchmarks.
Six Sigma is a quality improvement approach that calls for identification of causes of mistakes or
defects in organizational systems and processes. The paper elucidates the Six Sigma approach.
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CONSULTANCY FOR GAIN CERTIFICATION
STEPS TO GAINING CERTIFICATION
STEP 1 - PLANNING FOR SUCCESS
Obtaining certification against a BRC Global Standard may
represent a major challenge to some companies. It is therefore essential
that companies interested in becoming certificated consider carefully what
needs to be achieved prior to arranging a certification audit.
STEP 2 - GETTING PREPARED
Order a copy of the Standard and assess the compliance of your site to its
requirements. The BRC have published guidance documents on best
practice and on the use of standards for some sectors which may also be of
assistance.
To assist in the implementation of the BRC Global Standards, the BRC has developed a wide range of
practical training courses. Click here for further information.
STEP 3 - SELF ASSESSMENT
Review your current systems and practices against the requirements of the Standard in order to identify
areas which may need further work before undertaking a full audit. This can be carried out by your own
site, by a consultant familiar with the BRC Standard or by asking a Certification Body to undertake a
preassessment. Please note Certification Bodies are not able to provide consultancy although they can
identify areas where further work is required.
STEP 4 - SELECT A CERTIFICATION BODY
Select an accredited Certification Body to carry out the evaluation on your site. Only Certification Bodies
that are registered by the BRC can undertake audits. Certification Bodies can be selected by country by
clicking here.
Certification Bodies will require details of your site and operation before being able to provide a
quotation for the audit. Typical audit durations are indicated in the Standards.
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STEP 5 – AUDIT
A plan for the audit should be provided by your Certification Body to ensure that you and your team are
properly prepared. The audit may be extended if staff or documentation is not available at the audit so
preparation is essential. It is important that the site is in production at the time of the audit otherwise a
further audit will be required.
STEP 6 - CORRECTIVE ACTIONS
At the end of the audit the Certification Body should provide a written list of any areas which need
improvement in order to gain certification, this will also be discussed at the closing meeting. Where nonconformances have been identified, these must be addressed and suitable evidence provided to the
Certification Body for assessment within 28 days. In some circumstances it may be necessary for the
auditor to return to the site to check that appropriate corrective action has been taken.
STEP 7 - CERTIFICATION DECISION
The Certification Body will review the audit report from the auditor and corrective action documentation
provided in order to make a certification decision.
STEP 8 - ISSUE OF REPORT AND CERTIFICATE (IF APPLICABLE)
The audit report and certificate (if applicable) should be issued within 42 days of the original audit date
to the person who paid for the audit (usually the site). A copy of the report is automatically sent to the
BRC to allow quality control checking of the Certification Body undertaking the audit. Certificated sites
are invited to have site details placed on the BRC Directory website to advertise their achievements.
STEP 9 - ISSUE OF REPORT TO CUSTOMERS
It is a principle of the BRC scheme that the audit report is owned by the company paying for the audit
and copies can only be provided to other parties at the request of the owner (a copy is provided to the
BRC and this is held confidentially). It is usual to authorise the release of a copy of the report and/or
certificate for customers.
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SERVICES
CONSULTANCY FOR GREEN CERTIFICATION
If you look for GREEN things, if you really care for environmental
change, global warming, greenhouse
gases, recycling, CO2 emissions, carbon neutral, zero
carbon footprint, sustainable development, climate change,
compact fluorescent lights (CFL), compost, Al
Gore, and if you don't believe in Climate certification is for you.
GREEN CERTIFICATION ADVANTAGES:
Be a proud member of the GREEN Community
Show everyone that you really care for GREEN
Many other advantages that you can imagine by yourself!
Use the Official GREEN Logo on your certified products
The Requirements of Green Standard are assessed following International Standard ISO 14064
quantifying, monitoring and reporting Greenhouse Gases into Green Certificate Levels. Most credible
GHG and Project Methodologies, like CDM methodologies are used in validation and verification of
GHG emission reductions or removal enhancements.
Verified GHG emission reductions or removal enhancements fully support to voluntary carbon market.
Projects of Green Standard covers all carbon neutrality and social, economic and environmental
compliances – hence the products and services are ‘Green’
Forestry management; renewable energy sources use like Hydro, wind power, solar, biomass electricity
generation, methane utilization; energy efficiency technologies use like solar water heaters, cooking
system, biodigestors, LEDs; etc are some of GSCP supported low carbon technologies whilst Safe,
Healthy and Hygienic working environment and sound business compliances are b Approach
Green Certification is a ‘Clear Differentiator’ between businesses in the market reflecting
environmentally sound innovation and leadership.
Green Certificate strongly demonstrates organization’s ‘Corporate Social Responsibility (CSR)’ effort.
Organization can subscribe to any 'Level of Green Standard' based on their contribution Level-I, LevelII, Level-III.
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GREEN ORGANIZATION- LEVEL I
An organization awarded level I has demonstrated 26% to 50% compliance with the baseline
requirements of the green standard. Where the organization demonstrates 26% and above compliance
with the baseline, evidence of a reduction of GHG Emissions, exceeding compliances to regulatory
requirements, demonstrated efficient use of Product, Process, Resources and the use of recycled
material as per the Standard Requirement (See Requirements), the organization shall be Green
Organization complying Level I of the Green Standard.
GREEN ORGANIZATION- LEVEL II
An organization awarded level II has demonstrated 51% to 75% compliance with the baseline
requirements of the green standard. Where organization demonstrates 51% and above compliance with
the baseline, evidence of a reduction of GHG Emissions, exceeding compliances to regulatory
requirements, demonstrated an efficient use of Product, Process, Resources and the use of recycled
material as per the Standard Requirement (See Requirements), the organization shall be Green
Organization complying Level II of the Green Standard.
GREEN ORGANIZATION- LEVEL III
An organization awarded level III has demonstrated 76% to 100% compliance with the baseline
requirements of the green standard. Where the organization demonstrates 76% and above compliance
with the baseline, evidence of a reduction of GHG Emissions, exceeding compliance with regulatory
requirements, demonstrated an efficient use of Product, Processes, Resources and the use of recycled
material as per the requirements (See Requirements), the organization shall be Green Organization
complying Level III of the Green Standard.
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LISIONING FOR PRODUCT TESTING
KMS offers a full range of testing and certification services from
research and development, preproduction,
prototype, batch and audit to full compliance testing.
OUR SCOPE OF TESTING SERVICES:
CE Marking (CE Mark) Compliance
Direct Product Testing
We provide test report for above services through NABL & BIS
Approved Labs in India. Please visit our global site to find out more
information about the product testing services we provide.
We offer to our clients, highly efficient consultancy services to enable them to meet NABL requirements.
The concept of Laboratory Accreditation was developed to provide a means for third-party certification
of the competence of laboratories to perform specific type(s) of testing and calibration. Laboratory
Accreditation enhances customer confidence in accepting testing / calibration reports issued by
accredited laboratories.
The NABL is an autonomous body that has been established under the guidance of Department of
Science & Technology and Government of India. NABL provides certification on the basis of a
laboratory’s competence to perform specific testing & calibration thereby allowing customers to avail
reliable services. Our team of experts carefully analyzes the business of the clients and offers exact
consultancy services to fulfill NABL requirements.
The Product Testing process is associated with H/W and/or S/W releases which consists of the
following steps:
The service starts by helping the Customer organization to define the testing strategy based on
design specification, which results in a comprehensive Test Specification Document formally
reviewed by the Customer. Test specification document outlines all features and application
which have to be tested, what type of testing will be conducted during the test cycle and what
type of hardware requires for testing. The possible hardware-software interactions and
dependencies are identified during this step and result in separate or simultaneous test
processes for selected areas in the hardware.
Direct product testing is independent testing carried out directly with manufacturers or end
users. NABL Approved Labs can test against any published standard or client specification,
including performance specifications or governing bodies.
Direct testing need not necessarily lead to certification, for instance, the CE marking or ISI Mark
However, on completion of test work, we provide you with a detailed NABL Approved Lab Test
Report.
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The next step is to standardize the requirements into a series of Test Cases which typically numbers in
hundreds or even thousands that exhaustively exercise field usage under normal and marginal
situations. These test cases are collected in a Test Plan Document for Customer review and approval.
Test plan document ensures the testing of the core functionality of the system and all its features as will
be used when released to the field. Depending on the specific product functionality and customer
requirements, the testing may be automated so that it results in a faster, repeatable process for future
releases of the product software or it may be developed as a manual process.
Any possible anomaly detected in the execution of the Test Cases is documented and immediately
relayed to the Customer's Design Organization for correction.
Test Reports: The final results after bug correction are collected in a reference document called Final
Test Report.
OUR SCOPE OF TESTING IS:
All type of Electrical & Electronic Testing
All type of Mechanical Testing
All type of EMC Testing
All type of Rubber\Product Testing
All Type of Cables Testing
All Type of Personal Protective Equipment Testing
All Type of Fire product Testing
All Type of Construction product Testing
All Type of CE Product Testing
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TRAINING FOR ISO STANDARD
KMS offers a full range of Training and certification services
from research and development, pre-production, prototype,
batch and audit to full compliance Training.
This sample Training Needs Analysis tool shows general
competencies and behaviours examples. Free working files
versions, including individual assessments, are available at
businessballs.com, which you can adapt for your own job roles
and situations.
Using and developing my knowledge
Researching, investigating and problem-solving.
Communicating outwardly: face to face, phone, email,
etc.
Listening and interpretation, establishing rapport,
understanding needs.
Developing solutions and agreeing things with people.
Financial understanding and commercial ability.
Speaking and presenting to groups.
Helping or coaching or teaching or training others.
Using information and communications technology (ICT or IT).
Technical appreciation and use of equipment/tools/machinery for my area and related areas.
Understanding and making the most of my relationships with people and groups.
Competitor/industry awareness and consideration of these factors in planning, decision making,
etc.
Taking initiative and responsibility, e.g., decision-making, project management, running
meetings.
Visioning, creating, and inspiring others with my ideas.
Managing time, planning, being effective, efficient, productive, and reliable.
Appreciating/applying social responsibility, sustainability, humanity and ethical\ considerations.
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EXAMPLES OF BEHAVIOUR AND STYLE
Striving for personal development.
Taking personal responsibility to resolve problems, even those not of my own making.
Understanding the way people really feel.
Developing positive relationships.
Keeping focused and productive, reliable and dependable.
Planning how to achieve my work and personal goals.
Managing stress and conflict.
Managing upwards and sideways (my managerial superiors and my peers).
Contributing positively to team/company morale and spirit.
Seeking and picking up responsibility that I see waiting to be filled.
Team-working.
Having compassion and care for others.
Using integrity and ethics in my judgments about work and organizational
OUR SCOPE OF TRAINING IS:
ISO 9001:2008 ------- LEAD AUDITOR & INTERNAL AUDITOR
ISO 14001:2004 ------- LEAD AUDITOR & INTERNAL AUDITOR
OHSAS 18001:2007 ------- LEAD AUDITOR &INTERNAL AUDITOR
ISO 22000:2005 ------- LEAD AUDITOR & INTERNAL AUDITOR
ISO/HACCP ------- INTERNAL AUDITOR
cGMP ------- INTERNAL AUDITOR
ISO 10002 ------- INTERNAL AUDITOR
ISO 13485 ------- INTERNAL AUDITOR
ISO 20000 ------- INTERNAL AUDITOR
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ISO 27001 ------- LEAD AUDITOR & INTERNAL AUDITOR
ISO/TS 16949 (Includes 9001) ------- LEAD AUDITOR & INTERNAL AUDITOR
SA 8000 & SRM ------- INTERNAL AUDITOR
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LISIONING FOR CONTRACTOR OF DGS&D
DGS&D CERTIFICATION SERVICE
ADVANTAGES
TO SUPPLIERS:
Its REGISTRATION is held in high esteem by all Govt.
Department/Agencies
Award of rate contract lends respectability & image
enhancement
Marketing effort requires is nominal
Consistent & uniform purchase policies & procedures
Availability of technical guidance for upgrading
manufacturing processes & for building product quality
Uniform Quality Assurance techniques lead to standardization
Registered suppliers are given prior intimation about tenders
TO BUYERS:
Facility of bulk purchase of lowest competitive price
Enables buying as & when required
Saves effort involved in tedious & frequent tendering
Availability of quality goods with full quality assurance back-up
Just in Time availability of supplies for inventory management
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CONTRIBUTIONS TO THE NATIONAL ACTIVITIES:
TRANSPORTATION SECTION
Rails (inspects every metre of indigenous Rails used by Indian Railways)
Heavy Earth Moving Const. Equipment
Road construction & inspection machinery
Batteries, Tyres, Tubes
Spares for all types of vehicles & machinery
DRINKING WATER SUPPLY PROJECTS
All kinds of water carrying pipes like M.S. Galvanized Pipes, HDPE Pipes, CI spun Pipes,
Ductile iron Spun Pipes
Submersible Pumps
Hand Pumps
Drilling Rigs & accessories
Alumina Ferric & stable bleaching powder
Water Fittings like sluice valves
Air compressors
ORDINANCE FACTORIES
Production Machine Tools
Special purpose machines for arms & ammunition
CNC precision production/inspection & testing machines
PARA MILITARY FORCES (BSF, CRPF, ITBP, CISF, NSG, RAF)
Uniforms & Clothing
Tents, FRP Shelters & Camping Equipment
Communication Equipment like Transreceivers
Automobiles, Recovery Vehicles
Border Fencing & Lighting Equipment such as Concertina coils
Barbed wire, Night Vision Devices
Kitchen Equipment & Utensils
FIRE SERVICES
Crash fire tenders
Hydraulic Platforms/ Snorkels
Fire fighting equipment & documents
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HEALTH SERVICES
Drugs & Medicines
Specialized Hospital Equipment
Scanning Machines
PUBLIC UTILITIES (FOR CENTRAL & STATE GOVTS, CPWD, RAILWAYS, DEFENCE.
URBAN DEVELOPMENT)
Automobiles & spares
Generating Sets
Air Conditioners, Refrigerators, Water Coolers
Evaporative Air Coolers
Cables & conductors
Luminaries HPSV, HPMV, CFL, GLS Lamps, Fluorescent tubes & fittings
Electrical Accessories like MCBs, Switches, CSFU
Decorative laminates & rexine
Door & window fittings
Printing & copying machines like Digital copy printer, duplicating machines, photocopier
Household Electrical Appliances
Paper & Paper products
Cement
Bags for packing food grain
ENERGY CONSERVATION
Room air conditioners
Evaporative air cooler
Ballasts
Laminates electrical light fittings
Disaster Management
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LISIONING FOR CONTRACTOR OF NSIC
NSIC CERTIFICATION SERVICE
Raw Material Assistance Scheme aims at helping Small Scale
Industries/Enterprises by way of financing the purchase of Raw
Material (both indigenous & imported). This gives an opportunity
to SSI to focus better on manufacturing quality products.
Benefits of the Scheme
Financial Assistance for procurement of Raw Material upto 90
days.
SSI helped to avail Economics of Purchases like bulk
purchase; cash discount etc
NSIC takes care of all the procedures, documentation & issue of Letter of credit in case of imports.
For more details, kindly download the attached PDF.
http://2.imimg.com/data2/DG/OH/MY-/nsic.pdf
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FACTORY ASSESSMENT AND AUDIT SERVICES
FACTORY ASSESSMENT SERVICES
A factory assessment audits the production capability and
performance of a factory against proven quality principles.
As such, the key criteria assessed are policies, procedures
and records that would indicate the factory’s ability to deliver
consistent quality management over time, rather
than at one given time or only for certain products. Core
areas and processes addressed by a factory assessment
include:
Quality Management System
Good Manufacturing Practice (Factory Environment
Standards)
Product Control
Process Control
Personnel
WHAT ARE THE KEY BENEFITS?
OUR FACTORY ASSESSMENT SERVICES CAN HELP:
Evaluate capabilities of potential new vendors as part of the selection process
Identify key strengths and weaknesses of your existing vendor base
Monitor and track progress over time to drive quality throughout the manufacturing process
Provide an independent assessment tool that retailers, buyers and vendors can use together to
make improvements
You will receive a summary report and a score card report that will include both an overall score and
rating per section, highlighting key strengths and areas needing improvement. Our objective is to
provide measurable results to both vendors and retailers as they work together for shared success.
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Our factory assessments are designed to help retailers and vendors work together and improve
performance by providing detailed results that clearly indicate areas of strengths and opportunities. In
today’s market, as retailers and buyers are looking to select successful new vendors, reduce the
number of vendors to more manageable levels, and promote relationships that improve overall
performance, our assessment services provide an effective and unique method to help select and
enhance relationships. We offer:
A Best Practices Approach: Based on our experience in providing factory assessments for
multiple US based retailers, we have developed a ‘best practices approach’ that can save you
time and costs in creating and maintaining an effective factory assessment program.
Experienced Auditors: Our auditors receive comprehensive training including interpretation,
auditing techniques, report writing, audit planning, integrity and consistency.
A Strong Integrity & Ethics Program: With a reputation for strict ethical guidelines and
welltrained auditors, we maintain an active and dynamic training and integrity program that is
managed by a dedicated integrity team, in order to minimize the risks of corruption and to
educate auditors, factories and clients regarding our integrity policies and expectations.
Added-Value Assessments: In many cases, we have cross-trained our audit staff to conduct
factory assessments, social compliance and Security (C-TPAT) assessments. This gives you
the option of including additional value-added assessments that can benefit both you and your
suppliers.
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LISIONING FOR ISI MARK CERTIFICATION
The Bureau of Indian standards operates a product certification
scheme. The certification allows the licensees to use the popular
ISI Mark, which has become synonymous with quality product for
the Indian and neighboring markets. ISI Mark assures the user of
a product that it conforms to the requirements of relevant Indian
standard.
The BIS product certification scheme is essentially voluntary in
nature and is largely based on ISO Guide 28 which provides
general rules for third party certification system of determining
conformity with product standards.
If you wish to get ISI certification, please send us an enquiry.
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LISIONING FOR REGISTRATION FOR ALL TYPE OF INDUSTRIES
We take great pride in introducing ourselves as a leading law firm in
India, which has developed a high specialization in the field of
trademark registration in India. We cover all the requirements and
expectations of our global clients from our highly expertise trademark,
patent and company lawyers and attorneys beginning from Trademark
Search, Trademark Filing, Trademark oppositions, and Appeals,
trademark registration, international trademark registration services
and trademark enforcement services, which give complete customer
satisfaction completely.
KMS offer to all manufacturers & traders for Trademark
Registration, Logo Registration, Copy Right Registration, ®, ©, Patent,
Design, VAT, Service Tax, NGO, Trust, Society, Proprietor Ship Firm
Registration, Partnership Firm Registration, PVT.LTD, LTD, INDIA
LTD, Agmark, Hollmark, MCD, NBFC, 80G, 12A, IFCRA, PAN, PF,
ESI, TIN, TAN, Pollution Certificate, SSI, Direct & Indirect Taxation,
Bar Code, IE Code
TRADEMARK AND LOGO REGISTRATION SERVICE
We take great pride in introducing ourselves as a leading law firm in India, which has developed a high
specialization in the field of trademark registration in India. We cover all the requirements and
expectations of our global clients from our highly expertise trademark, patent and company lawyers and
attorneys beginning from Trademark Search, Trademark Filing, Trademark oppositions, and Appeals,
trademark registration, international trademark registration services and trademark enforcement
services, which give complete customer satisfaction completely. We have a team of highly qualified and
experienced professionals, who are expert in solving all types of issues related to trademark
registration. Our policy is to enhance the customer satisfaction through providing high quality trademark
registration services and query resolution system.
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TRADEMARK SEARCH:
A trademark search is an analytical and comprehensive way of researching a name, logo or slogan for
prior use. It is highly advisable to conduct a trademark search before filing an application for a
trademark. A basic trademark search includes applications for trademarks in India and registered
trademarks. This search is only for required and relevant information, but every possible effort has been
made to ensure accurate results. The main purpose of a trademark search is to determine if someone
has already trademarked your intended mark.
PATENT REGISTRATION
We are specialized to deliver patent registration, patent filing, international patent registration, and
international patent filing services at affordable price to our global clients in India & across the globe.
We have a team of highly qualified and experienced professional, who can assist you in providing
quality patent registration services and query resolution system.
PCT FILING
The Patent cooperation Treaty is an agreement for international cooperation in the field of the patents
which provides easy and affordable procedure for filing patent applications. Mainly, It is a treaty for
rationalization and cooperation with regard to the PCT filing procedure, searching and examination of
patent applications and the dissemination of the technical information contained therein.
We provide specialized solutions for national and international patent filing to our clients, which suit the
client's requirements and expectations completely. Our experienced professionals can help you in
providing easy and affordable procedure for pct filing, which meet your needs completely.
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LISIONING FOR FPO & MFPO
MFPO REGISTRATION IS AVAILABLE
FOR FOLLOWING PRODUCTS :
In this order, unless, the context otherwise requires (a)“animal”
means an animal belonging to any of the species specified below:
Ovines;
Caprines;
Suillines;
Bovines;
and includes poultry;
(b)“carcass” means the dead body or any part thereof including the
viscera of any animal which has been slaughtered;
(c) “Committee” means the Meat Food Products Advisory Committee constituted under clause 3;
(d)“factory” means any premises including the precincts thereof, wherein meat food products are
manufactured or packed for sale;
(e) “licensee” means a manufacturer to whom a license is granted under this order;
(f) “licensing authority” means the Agricultural Marketing Adviser to the Government of India and
includes any other officer authorised by him in this behalf with the previous approval of the Central
Government;
(g)“local authority” means a municipal council, committee, corporation, panchayat, notified area
committee or other authority entrusted with the regulation and licensing of slaughter houses in any local
area;
(h)“Manufacturer” means a person engaged in the business of manufacturing, packing, repacking,
relabeling meat food products meant for sale, but shall not include a person who manufactures such
products and serves on the spot for consumption in a restaurant, hotel, boarding house, snack bar,
eating house or any other similar establishment;
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(i)“meat” means the flesh and other edible parts of a carcass;
(j)“meat food products” means any article of food or any article intended for, or capable of, being used
as a food which is derived or prepared from meat by means of drying, curing, smoking, cooking,
seasoning, flavorings or following a method of processing meat akin to any of the above methods, but
shall not include the following products unless the manufacturer himself desires to be covered under the
provisions of the said order, namely:Meat extracts, meat consommé and stock, meat sauces and similar products not containing
fragments of meat;
Whole, broken or crushed bones, meat peptones, animal gelatin, meat powder, pork-rind
powder, blood plasma, dried blood, dried blood plasma, cellular proteins, bone extracts and
similar products;
Fats melted down from animal tissues;
Stomachs, bladders and intestines, clean and bleached, salted or dried;
(v) Products containing fragments of meat, but which contain a quantity of meat or meat product
not exceeding ten percent of the total weight of the final product;
Patties, puffs, rolls, samosas, cutlets, koftas, kababs, chops, tikkas and soups made from
mutton, chicken, goat meat, buffalo meat, beef and grilled chicken which are prepared for
immediate consumption, the ampoules of chicken essence, hot-dogs and hamburgers prepared
for immediate consumption which can not be stored even under refrigerated conditions;
(k) “Meat Food Products Inspector” means an official veterinarian appointed by the licensing authority
and includes any officer of a local authority authorised to perform the functions of the Meat Food
Products Inspector under this Order;
(l) “Schedule” means a Schedule appended to this Order;
(m) “Slaughter house” means the building, premises or place which is licensed as a slaughter house by
the local authority for the slaughter of animals intended for human consumption.;
(n) “Year” means a calendar year or part thereof.
FPO REGISTRATION IS AVAILABLE FOR FOLLOWING PRODUCTS :
Synthetic beverages syrups and sharebats, Vinegar whether brewed or syntheric, Pickles, Dehydrated
Fruits and Vegetables, Squashes crushes, Cordials, Barley water baralled juice and ready to serve
beverages fruit sector, or any other beverages containing fruit juices or fruit pulp, Jams, Jelleys and
marmalades, Tomato products, ketchup and sauces, Preserves candid and crystallized fruit and peels,
Chatnies, Cancel and bottled fruits juices and pulp, Canned and bottled Vegetables, Frozen fruits and
vegetables Sweetened arreated waters with or without fruit juices or fruit pulp, Fruit cereal flakes, any
other unspecified item relating to fruits or vegetables etc.
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REQUIREMENT FOR FPO APPLICATION PROCEEDINGS
Copy of test report(s), duly authenticated, from independent FPO recognized laboratory.
Document authenticating establishment of the firm, such as Registration by Company Registrar OR
State Authority or Memorandum of Article in case Applicant Firm is a Limited Company OR Partnership
Deed in case the applicant firm is under Partnership.
Name of the products /Item.
Name of the applicant
Name of the Firm/ Company
Address of the Firm/ Company
Sample of the product(in pouch of 500gm.1kg.
Started Time period of product(specify exact Date/Month/year)
Total gross product in K.g.(for last year)
Turnover of last year
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TIE UP WITH LOTS OF ACCREDITED CERTIFICATION BODIES
We are engaged in offering following Accreditation Board Certifications to our clients. We offer
United Kingdom Accreditation Service, American National Accreditation Board, National
Accreditation Board for Certification Bodies, International Automotive Task Force, Worldwide
Responsible Apparel Production, IRCA International Register for Certificated Auditor, Bureau
of Indian Standard (BIS), India, NORWAY Accreditation Board, JAS ANZ Accreditation Board,
Turkey Accreditation Board.
UNITED KINGDOM ACCREDITATION
SERVICE
UKAS was the first body formed for assessing and
accrediting the Competence of Organizations.
UKAS Accredits certification for ISO 9001, ISO
14001, ISO 13485, ISO27001, ISO22000, AS9100
etc.
AMERICAN NATIONAL
ACCREDITATION BOARD
ANAB is a US Accreditation Body for
Management Systems Certifications. ANAB has
Accredited certification for ISO 9001 (QMS)
Certifications.
NATIONAL ACCREDITATION BOARD
FOR CERTIFICATION BODIES
NABCB is a Constituent of Quality Council of India
and is Member of MLA. NABCB has Accredited
Certification in the Area of ISO 9001(QMS)
Certifications.
INTERNATIONAL AUTOMOTIVE TASK
FORCE
IATF is the Sole Accreditation Board in the
World providing Recognition to CBs for TS
16949 Certification to Automotive Supply Chain.
Certification Bodies which is given the
certification is Recognized from IATF for ISO/TS
16949 Certification.
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NORWAY ACCREDITATION BOARD
We offer the Certification for ISO 9001, ISO 14001
through Norway Accredited
Certification Body
JAS ANZ ACCREDITATION BOARD
We offer the Certification for ISO 9001, ISO
14001 through JAS-ANZ Accredited Certification
Body.
TURKEY ACCREDITATION BOARD
We offer the Certification for ISO 9001, ISO 14001,
ISO 22000 through Turkey Accredited Certification
Body
WORLDWIDE RESPONSIBLE APPAREL
PRODUCTION
WRAP is an Independent, Non-Profit
Organization dedicated to the Certification of
Lawful, Humane and Ethical Manufacturing
throughout the World. We conduct Certification
Monitoring in Key Sourcing Countries Accredited
by the Worldwide
Responsible
Apparel
Production for WRAP Certification in Industries
like Apparel, Footwear.
IRCA INTERNATIONAL REGISTER
FOR CERTIFICATED AUDITOR
IRCA certified Auditor Training is Recognized and
Respected Internationally for providing Industry
Accepted to those wanting to become IRCA
Certificated Auditors and also for assisting
Professionals who wish to acquire Competence in
Auditing and Management Systems Standards.
Our Lead Auditor Trainings for QMS, EMS, FSMS
are Accredited by IRCA.
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