CERTIFICATIONS

IATF 16949:2016

WHAT IS IATF 16949:2016?

In October 2016 IATF 16949:2016 will be published by IATF and will supersede and replace the current ISO/TS 16949, defining the requirements of a quality management system for organizations in the automotive industry. It will be aligned with and refer to the most recent version of ISO’s quality management systems standard, ISO 9001:2015

IATF

IATF 16949:2016 will fully respect ISO 9001:2015 structure and requirements. IATF 16949:2016 is not a stand-alone quality management standard, but is implemented as a supplement to, and in conjunction with, ISO 9001:2015. The International Automotive Task Force, IATF, has developed its own unique and proprietary registration process and requirements for organization registration, and conducts its own qualifying of certification bodies/registrars and their auditors.

The primary focus of the IATF 16949 standard is 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. The standard, combined with applicable Customer-Specific Requirements (CSR’s), define the QMS requirements for automotive production, service and/or accessory parts.

IATF 16949:2016 will fully respect ISO 9001:2015 structure and requirements. IATF 16949:2016 is not a stand-alone quality management standard, but is implemented as a supplement to, and in conjunction with, ISO 9001:2015. The International Automotive Task Force, IATF, has developed its own unique and proprietary registration process and requirements for organization registration, and conducts its own qualifying of certification bodies/registrars and their auditors.

The primary focus of the IATF 16949 standard is 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. The standard, combined with applicable Customer-Specific Requirements (CSR’s), define the QMS requirements for automotive production, service and/or accessory parts.

WHAT INCLUDED IN IATF 16949:2016 STANDARD?

ISO 9001:2015 requirements.
Automotive Industry Action Group Requirements (It is called core tools).
SPC – Statistical Process Control.
MSA – Measurement System Analysis
FMEA – Failure Mode and Effects Analysis
PPAP – Production Part Approval Process
APQP – Advanced Product Quality Planning
IATF 16949:2016 requirements.
Customer specific requirements.

WHO CAN APPLY FOR ISO 9001?

It can be used by any supplier, large or small, and should be applied throughout the automotive supply chain

WHAT INCLUDED IN IATF 16949:2016 STANDARD?

Visit / understand client requirement.
Offer communication to client.
Offer acceptance and gap analysis.
Kick off meeting with detailed time plan i.e. roadmap.
IATF 16949:2016 awareness Training.
Preparation of quality manual/procedure.
Core tools trainings (SPC, MSA, FMEA, PPAP, APQP).
IATF 16949:2016 internal auditor certification.
Preparation of documented information for all departments.
internal audit and plan for corrective and preventive action.
Conduct stage-I audit and stage-II audit.
Certification follow-up.

BENEFITS OF IATF 16949 CERTIFICATION:

Reduction of variation and waste in the supply chain.
Continual improvement focus.
Generates new business opportunities.
Enhancing product quality.
Reduce error / defect.
Reduce the business/ product risk.
Improving overall traceability.
Use fact and data to drive better solution.

ISO 9001:2015 - QUALITY MANAGEMENT SYSTEMS

WHAT IS ISO 9001:2015?

ISO 9001 is the internationally accepted quality management system, which will help the organization to drive systematic way of quality management. The purpose of ISO 9001 is to facilitate international trade by providing a single standard that is recognized and respected globally, ISO 9001 certification is suitable for all sizes and types of organizations and is well established around the world as an invaluable Quality Management System standard. Quality management systems optimize production processes/services, increase efficiency and reduce costs.

ISO 9001

The ISO 9001 certificate indicates the organization’s adherence to quality management practices and minimizes the potential risk to customers. These good practices are compiled into a set of standardized requirements for a quality management system for your organization. ISO 9001:2015 is important because of its international acceptance. It is recognized in more than 120 countries and is the logical choice for any organization involved in international business or committed to quality. Quality management provides framework which assures products and services satisfy the customer’s quality requirements and comply with all the regulations applicable to those products or services.

WHO CAN APPLY FOR ISO 9001?

It is suitable for organizations in all industry sectors and will help your organization to improve management processes to compete locally and/or globally. Who need to improve the systematic quality can apply?

HOW TO VALIDATE ORIGINAL ISO CERTIFICATE?

The certificate issued by a certification body bearing the accreditation mark of a recognized IAF MLA (international Accreditation Forum Multilateral Recognition Arrangement) member and where the accreditation body’s main scope includes management system certification to ISO/lEC1702l.

HIGHLIGHTS OF ISO 9001 STANDARDS INCLUDED?

The ISO 9001:2015 standards aligned with 10 clauses to ensure greater harmonization among its many different management system standards. The new ISO 9001:2015 standard includes three basic core concepts:

process approach
plan-do-check act methodology, and
which is new in the 2015 version is risk-based thinking

More focus on risk-based customer focus, Quality objective as per ISO 9001:2015 certification is seen as those that have a direct impact on customer requirements, have a direct impact of the efficiency of the client’s business, which means an improvement in the quality system processes. ISO 9001:2015 standard requires quality objectives to be measurable which means that targets have to be set. The requirements around the ISO 9001:2015 objectives have also been made more detailed. They are to be consistent with the ISO 9001:2015 quality policy, measurable (if practicable), monitored, communicated, and updated as appropriate. They have to be established at relevant functions and levels. Now planning how to achieve its quality objectives is introduced in the new version of ISO 9001:2015 standard.

BENEFITS OF ISO 9001 CERTIFICATION

Generates new business opportunities.
Enhancing product quality.
Reduce error / defect.
Reduce the business/ product risk.
Improving overall traceability.
Use fact and data to drive better solution.
Continual improvement focus.

ISO 9001 CERTIFICATION PROCEDURE:

Visit / understand client requirement.
Offer communication to client.
Offer acceptance and gap analysis.
Kick off meeting with detailed time plan i.e. roadmap.
ISO 9001:2015 awareness Training.
Preparation of quality manual/procedure.
ISO 9001:2015 internal auditor certification.
Preparation of documented information for all departments.
Conduct internal audit and plan for corrective and preventive action.
Conduct stage-I audit and stage-II audit.
Certification follow-up.

ISO 14001:2015 - ENVIRONMENTAL MANAGEMENT SYSTEMS

WHAT IS ISO 14001:2015?

ISO 14001 is an internationally agreed standard that sets out the requirements for an environmental management system. It helps organizations improve their environmental performance through more efficient use of resources and reduction of waste, gaining a competitive advantage and the trust of stakeholders. The ISO 14001 Environmental management system (EMS) refers to the management of an organization’s environmental programs in a comprehensive, systematic, planned and documented manner.

ISO 14001

It includes the organizational structure, planning and resources for developing, implementing and maintaining policy for environmental protection. Environmental management systems certification enables an organization to demonstrate its commitment to the environment. The standard provides guidance on how to manage the environmental aspects of your business activities more effectively, while taking into consideration environmental protection, pollution prevention and socio-economic needs.

Increased awareness of sustainable development and production gives environmentally credible companies a competitive edge in national and international markets. A certified Environmental Management System proves that your business is taking active steps to fulfil your environmental responsibilities.

ISO 14001 compliance can also provide your company with a better use of energy and resources, and reduce costs over time. It also assists you to ensure compliance with environmental legislation and reduces the risk of penalties and possible litigation.

WHO CAN APPLY ISO 14001:2015?

ISO 14001:2015 is applicable to any organization, regardless of size, type and nature, and applies to the environmental aspects of its activities, products and services that the organization determines it can either control or influence considering a life cycle perspective.

STEPS TO GET ISO 14001 CERTIFICATION:

Visit / understand client requirement.
Offer communication to client.
Offer acceptance and gap analysis.
Kick off meeting with detailed time plan i.e. roadmap.
ISO 14001:2015 awareness Training.
Preparation of quality manual/procedure.
ISO 14001:2015 internal auditor certification.
Preparation of documented information for all departments
Conduct internal audit and plan for corrective and preventive action.
Conduct stage-I audit and stage-II audit.

BENEFITS OF ISO 14001 CERTIFICATION:

Demonstrate compliance with current and future statutory and regulatory requirements.
Encourage better environmental performance of suppliers by integrating them into the organization’s business systems.
Increase leadership involvement and engagement of employees.
Preventing the organization for potential adverse effect of environmental conditions on the organization.

ISO 45001:2018 – OCCUPATION HEALTH & SAFETY

ISO 45001 is an International Standard that specifies requirements for an occupational health and safety (OH&S) management system, with guidance for its use, to enable an organisation to proactively improve its OH&S performance in preventing injury and ill-health. ISO 45001 is an ISO standard for management systems of occupational health and safety (OH&S), published in March 2018. The standard is based on OHSAS 18001, conventions and guidelines of the International Labour Organization including ILO OSH 2001, and national standards.

ISO 45001

Organizations that implement ISO 45001 have a clear management structure with defined authority and responsibility, clear objectives for improvement, with measurable results and a structured approach to risk assessment. This includes the monitoring of health and safety management failures, auditing of performance and review of policies and objectives.

WHO CAN APPLY FOR ISO 45001:2018?

The standard is applicable to any organization that wishes to eliminate or minimize risk to employees and other stakeholders who may be exposed to OH&S risks associated with its activities.

DEFINED ACTIVITY TO ISO 45001 CERTIFICATION

Visit / understand client requirement.
Offer communication to client.
Offer acceptance and gap analysis.
Kick off meeting with detailed time plan i.e. roadmap.
ISO 45001:2018 awareness Training
Preparation of quality manual/procedure.
ISO 45001:2018 internal auditor certification.
Preparation of documented information for all departments
Conduct internal audit and plan for corrective and preventive action.
Conduct stage-I audit and stage-II audit.
Certification follow-up.

BENEFITS OF ISO 45001 CERTIFICATION:

Improving its ability to respond to regulatory compliance issues.
Reduce the exposure of employees and other parties to occupational health and safety risks associated with the organizations activities.
Greater assurance of conformance with occupational health and safety policy.

ISO 13485:2016 MEDICAL DEVICES — QUALITY MANAGEMENT SYSTEMS —

REQUIREMENTS FOR REGULATORY PURPOSES

ISO 13485:2016 specifies requirements for a quality management system that can be used by an organization involved in one or more stages of the life-cycle of a medical device, including design and development, production, storage and distribution, installation, servicing, final decommissioning, disposal of medical devices.

ISO 13485

ISO 13485:2016 can also be used by suppliers or other external parties providing product like raw materials, components, subassemblies, medical devices, sterilization services, calibration services, distribution services, maintenance services. The supplier or external party can voluntarily choose to conform to the requirements of this International Standard or can be required by contract to conform.

ISO 27001:2013 - INFORMATION SECURITY MANAGEMENT

WHAT IS ISO 27001:2013?

ISO 27001:2013 is the internationally recognised best practice framework for an Information Security Management System (ISMS). It is one of the most popular information security standards worldwide.

ISO 27001

ISO 27001 (formally known as ISO/IEC 27001:2005) is a specification for an information security management system (ISMS). An ISMS is a framework of policies and procedures that includes all legal, physical and technical controls involved in an organization’s information risk management processes. According to its documentation, ISO 27001 was developed to provide a model for establishing, maintaining and improving an information security management system. ISO 27001 uses a top down, risk-based approach and is technology-neutral.

ISO 27001 certification demonstrates that you have identified the risks, assessed the implications and put in place systemised controls to limit any damage to the organisation. Benefits include: Increased reliability and security of systems and information. Improved customer and business partner confidence.

WHAT INCLUDED IN ISO 27001:2013:

The specification defines a six-part planning process:
Define a security policy.
Define the scope of the ISMS.
Conduct a risk assessment.
Manage identified risks.
Select control objectives and controls to be implemented.
Prepare a statement of applicability.

The specification includes details for documentation, management responsibility, internal audits, continual improvement, and corrective and preventive action. The standard requires cooperation among all sections of an organization.

BENEFITS OF ISO 27000 CERTIFICATION

Increased reliability and security of systems and information.
Improved customer and business partner confidence.
Increased business resilience.
Alignment with customer requirements.
Improved management processes and integration with corporate risk strategies.
Increase the ability to comply with the GDPR (General Data Protection Regulation) approved by EU.

PROCESS STAGES

Some of the stages you will need to go through to protect your business and achieve ISO 27001 include:

Assessing the potential risks to your business and identifying areas that are vulnerable.
Implementing a management system that covers the entire organisation will help to control how and where information is stored and used.
Maintaining a process to manage current and future information security policy.
Making employees and third party contractors aware of the risks and incident reporting.
Monitoring system activity and logging user activities.
Keeping IT systems up to date with the latest protection.
System access control.

ISO 22000:2005 - FOOD SAFETY MANAGEMENT

WHAT IS ISO 22000?

The ISO 22000 family of International standards addresses food safety management. ISO 22000 standard 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. This International Standard specifies requirements to enable an organization. All requirements of this International Standard are generic and are intended to be applicable to all organizations in the food chain regardless of size and complexity.

ISO 22001

This includes organizations directly or indirectly involved in one or more steps of the food chain. Organizations that are directly involved include, but are not limited to, feed producers, harvesters, farmers, producers of ingredients, food manufacturers, retailers, food services, catering services, organizations providing cleaning and sanitation services, transportation, storage and distribution services. Other organizations that are indirectly involved include, but are not limited to, suppliers of equipment, cleaning and sanitizing agents, packaging material, and other food contact materials.

WHO CAN APPLY FOR ISO 22000?

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.

WHAT INCLUDED IN ISO 22000

The standard combines four key elements to ensure food safety along the food chain, including: Interactive communication, System management, Control of food safety hazards through pre-requisite programmes and HACCP plans.

BENEFITS OF ISO 22000 CERTIFICATION:

For consumers:

  • conformity of products and services to International standards.
  • Provides assurance about:

-Quality
-safety
-Reliability
How ISO 22000 benefit society?

  • This, in turn, means that businesses using ISO 22000 are increasingly free to compete on many more markets around the world.
  • For businesses, the widespread adoption of ISO 22000 means that suppliers can base the development of their products and services on specifications that have wide acceptance in their sectors.

How ISO 22000 benefit developing countries?

  • For developing countries, ISO 22000 represents an international consensus and constitute an important source of technological know-how;
  • By defining the characteristics that products and services will be expected to meet on export markets;
  • International Standards give developing countries a basis for making the right decisions when investing their scarce resources and thus avoid squandering them

AS 9100 – Aerospace QMS

WHAT IS AS 9100?

AS 9100 is the US version of a globally harmonized quality management system standard, based upon the internationally renowned ISO 9001 quality management system. It supplements ISO 9001, focusing upon the unique, complex, and highly regulated nature of the aerospace industry. Specifically, it emphasizes the critical aspects of key characteristics and the need to satisfy internal, governmental and regulatory requirements. The global nature of the standard allows commonality throughout the industry, allowing increased trade and co-operation.

AS 9100

The standard, which is supported by the leading global aerospace organizations, is based around organizational processes. As with ISO 9001, the core concept is the Plan-Do-Check-Act cycle, which focuses the organization on its key processes. The model also builds in the ideas of planning, and reviewing, and that organizations should continually improve.

Benefits of AS 9100

Focuses the organization upon the key requirements of the customer
Focuses the organization upon the key characteristics of aerospace products and services
Demonstrates the operation of globally accepted quality standards
Increased opportunities and acceptance within the global aerospace supply-chain
Improved product and process quality
Reassignment of supplier resources to quality improvement
Potential reduction in variation of quality
Efficiency gains
Compliance with a system supported by regulatory bodies
Potential reduction in 2nd party system audits
Excellent levels of traceability throughout the supply chain
Common language to improve understanding of quality requirements

SA 8000 Social Accountability

WHAT IS SA 8000?

The SA8000 standard and verification system is a credible, comprehensive and efficient tool for assuring humane workplaces because it includes:
Factory-level management system requirement for ongoing compliance and improvement.

SA 8000

Independent, expert verification of compliance: Certification of facilities by auditing bodies accredited by SAI. SAI accreditation ensures that auditors have the procedures and resources needed to conduct thorough and objective audits. There are currently nine organizations accredited to do SA8000 certification.

Involvement by all stakeholders: Participation by all key sectors, including workers and trade unions, companies, socially responsible investors, nongovernmental organizations and government, in the SA8000 system. Such participation is required with the Advisory Board, drafting and revision of the standard and auditing system, conferences, training, and the complaints system.

Public reporting: SA8000 certified facilities are posted on the SAI Web site. Companies that join level two of the SA8000 Corporate Involvement Program (CIP) release annual progress reports verified by SAI.

Harnessing consumer and investor concern: The SA8000 Certification and Corporate Involvement Program help consumers and investors to identify and support companies that are committed to assuring human rights in the workplace SA8000 Standard Elements.

BENEFITS OF SA 8000

Along with humane workplaces, the implementation of SA8000 offers more benefits to workers, companies and others:
Benefits for Workers, Trade Unions and NGOs:

– Enhanced opportunities to organize trade unions and bargain collectively.
– A tool to educate workers about core labor rights.
– An opportunity to work directly with business on labor rights issues.
– A way to generate public awareness of companies committed to assuring humane working conditions.

Benefits for Business:

– Drives company values into action.
– Enhances company and brand reputation.
– Improves employee recruitment, retention and productivity.
– Supports better supply chain management and performance.

Benefits for Consumers and Investors:

– Clear and credible assurance for ethical purchasing decisions.
– Identification of ethically made products and companies committed to ethical sourcing.
– Broad coverage of product categories and production geography.

Implementing a SA 8000

Purchase the Standard.
Review support literature and software.
Assemble a team and agree on your strategy.
Consider Training.
Review Consultancy Options.
Choose a registrar.
Develop a SA 8000 manual.
Develop support documentation.
Implement your SA 8000.
Consider a pre-assessment.
Gain registration.
Continual assessment.

ISO/TS 22613 – IRIS – Rail QMS

What is ISO/TS 22613-IRIS?

IRIS stands for International Railway Industry Standard. It is a globally recognized standard unique to the railway sector for the evaluation of management systems.

The IRIS Certification® Conformity assessment:2020 are owned by UNIFE (Association of European Railway Industries )and contain all the relevant rules relating to assessment methodology and the certification process. IRIS (International Railway Industry Standard) is only applicable to Rolling Stock and Signaling companies having
manufacturing and/or
design and/or
maintenance activities.

ISO

The ISO/TS 22163:2017 is owned by ISO. It contains the requirements of the ISO 9001:2015 Standard and the supplemental rail-specific requirements.

The ISO/TS 22163 contains the business Management requirements for rail organizations.

It is based on the ISO 9001:2015 and includes specific application requirements for rail organizations in areas of project management, change and configuration management, and competences.

The standard covers the entire bidding, development and production processes – ranging from the delivery of supplies to production to delivery of the final product – considering the scheduling as well as qualitative criteria.

What we do in ISO/TS 22163 - IRIS Certification ?

Turnkey projects on IRIS Certification Consultancy Services
Awareness Training
Implementation Training
Internal Auditor Training
Training on RAMS / LCC
Training on Project Management
Handholding services of IRIS Certification process

Our Visitor

005106
<p>This is the sidebar content, HTML is allowed.</p>