hrdcorp Malaysia, Selangor, Kuala Lumpur (KL), Puchong
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 IATF 16949:2016 AUTOMOTIVE QUALITY MANAGEMENT SYSTEMSIATF 16949, in conjunction with ISO 9001, defines the quality management system requirements for the design and development, production and, when relevant, installation and service of automotive-related products.
IATF 16949 is applicable to sites of the organization where customer-specified parts, for production and/or service, are manufactured.
Supporting functions, whether on-site or remote (such as design centres, corporate headquarters and distribution centres), form part of the site audit as they support the site, but cannot obtain stand-alone certification to IATF 16949.
IATF 16949 can be applied throughout the automotive supply chain.
Requirements of IATF 16949:2016
• Scope
• Normative Reference
• Terms and Definitions
• Quality Management System
• Management Responsibility
• Resource Management
• Product realization
• Measurement, analysis and improvement
Benefits of IATF 16949:2016
• Gain your licence to trade internationally and expand your business
• Improve processes to reduce waste and prevent defects
• Remove the need for multiples certificates for vehicle manufacturing
• Integrate IATF 16949 with other management systems
• Demonstrate compliance to win new business and investment prospects
How can ELITE assist you?
ELITE provides IATF 16949 management systems training and consultancy services. We offer specialized expertise and extensive practical experience to assist client in developing management systems from the initial concept to establishment and successful implementation of the management systems.
We use the following consultation approach to assist you in achieving certification:
1. Identify areas requiring improvement or development within your current Management Systems
2. Prepare a strategic action plan, in conjunction with your company personnel, to address those improvement areas and assist with the communication of these requirements to key personnel at all levels
3. Provide system-related trainings for your company personnel to create awareness and provide them with the necessary knowledge and skills in the implementation of systems
4. Provide assistance and advice on the development and implementation of systems, including preparation of documentation
5. Advise and assist, if required, with the preparation and submission of applications to your certification body
6. Assist with the development of internal auditing procedures and training
7. Conduct internal audit to ensure the effective implementation of the management systems prior to final audit by your certification body
8. Conduct Management Review Meeting to review performance of management systems and identify areas for improvement prior to final audit by your certification body
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 ISO/IEC 17025:2017 GENERAL REQUIREMENTS FOR THE COMPETENCE OF TESTING AND CALIBRATION LABORATORIESISO/IEC 17025:2017 General Requirements for the Competence of Testing and Calibration Laboratories
General requirements for the competence of testing and calibration laboratories is the main ISO standard used by testing and calibration laboratories. In most major countries, ISO/IEC 17025 is the standard for which most labs must hold accreditation in order to be deemed technically competent. Requirements of ISO/IEC 17025
• Clause 4 General requirements Benefits of ISO/IEC 17025
• Enables laboratories to demonstrate that they operate competently and generate valid results, thereby promoting confidence in their work both nationally and around the world. How can ELITE assist you?
We provide ISO/IEC 17025 standard training and consultancy services. We offer specialized expertise and extensive practical experience to assist client in developing management systems from the initial concept to establishment and successful implementation of the management systems. |
 ISO 45001:2018 OCCUPATIONAL HEALTH AND SAFETY MANAGEMENT SYSTEMS
ISO 45001:2018 replaces OHSAS 18001:2007 as the globally recognized occupational health and safety management system certification standard. While it is similar to OHSAS 18001, the new ISO 45001 standard adopts the Annex SL top-level framework of all new and revised ISO management system standards
Transition from OHSAS 18001:2009 to ISO 45001:2018
ISO 45001 is anticipated to replace OHSAS 18001 over three years following its publication. It uses the management system standard structure guideline Annex SL to allow for simplified integration with other management system standards, such as ISO 9001 and ISO 14001.
How to make the transition?
• Obtain a copy of ISO 45001:2018.
• Identify the gaps in your existing OHSAS 18001 system which need to be addressed to meet any new requirements.
• Develop an implementation plan.
• Ensure that any new competence needs are met and create awareness for all parties that have an impact on the effectiveness of the OHSAS.
• Update the existing OHSAS to meet the new requirements and provide verification of its effectiveness.
• Where applicable, liaise with your certification body for migration arrangements.
Benefits of ISO 45001:2018
• Improve employees morale and safety
• Savings in cost for insurance premiums
• Reduced occupational health & safety risks
• Prevention of potential accidents and ill health
• Enhance reputation among regulators, customers and public
How can ELITE assist you?
ELITE provides ISO 45001 management system training and consultancy services. We offer specialized expertise and extensive practical experience to assist client in developing management systems from the initial concept to establishment and successful implementation of the management systems.
We use the following consultation approach to assist you in achieving certification:
1. Identify areas requiring improvement or development within your current Management System
2. Prepare a strategic action plan, in conjunction with your company personnel, to address those improvement areas and assist with the communication of these requirements to key personnel at all levels
3. Provide system-related trainings for your company personnel to create awareness and provide them with the necessary knowledge and skills in the implementation of systems
4. Provide assistance and advice on the development and implementation of systems, including preparation of documentation
5. Advise and assist, if required, with the preparation and submission of applications to your certification body
6. Assist with the development of internal auditing procedures and training
7. Conduct internal audit to ensure the effective implementation of the management system prior to final audit by your certification body
8. Conduct Management Review Meeting to review performance of management system and identify areas for improvement prior to final audit by your certification body
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 ISO 22000:2018 FOOD SAFETY MANAGEMENT SYSTEMS
ISO 22000:2018 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. 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.
Requirements of ISO 22000:2018
• Scope
• Normative Reference
• Terms and Definitions
• Context of the Organization
• Leadership
• Planning for the Food Safety Management System
• Support
• Operation
• Performance Evaluation
• Improvement
How can ELITE assist you?
ELITE provides food safety management system training and consultancy services. We offer specialized expertise and extensive practical experience to assist client in developing management systems from the initial concept to establishment and successful implementation of the management systems.
We use the following consultation approach to assist you in achieving certification:
1. Identify areas requiring improvement or development within your current Management System
2. Prepare a strategic action plan, in conjunction with your company personnel, to address those improvement areas and assist with the communication of these requirements to key personnel at all levels
3. Provide system-related trainings for your company personnel to create awareness and provide them with the necessary knowledge and skills in the implementation of systems
4. Provide assistance and advice on the development and implementation of systems, including preparation of documentation
5. Advise and assist, if required, with the preparation and submission of applications to your certification body
6. Assist with the development of internal auditing procedures and training
7. Conduct internal audit to ensure the effective implementation of the management system prior to final audit by your certification body
8. Conduct Management Review Meeting to review performance of management system and identify areas for improvement prior to final audit by your certification body
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 ISO 14001:2015 ENVIRONMENTAL MANAGEMENT SYSTEMS
ISO 14001:2015 sets out the criteria for an environmental management system. It maps out a framework that a company or organization can follow to set up an effective environmental management system to help reduce the impact of its business to the environment. It also provides assurance to the company management as well as stakeholders of its commitment to monitor and measure its environmental performance. It can be used by any organization regardless of its activity or sector.
Requirements of ISO 14001:2015
• Scope
• Normative Reference
• Terms and Definitions
• Context of the Organization
• Leadership
• Planning
• Support
• Operation
• Performance Evaluation
• Improvement
Benefits of ISO 14001:2015
• Reduced cost of waste management
• Savings in consumption of energy and materials
• Systematic approach in addressing environmental protection
• Continual improvement of environment management system to prevent pollution
• Improved corporate image among regulators and environmentally aware customers
How can ELITE assist you?
ELITE provides management system training and consultancy services. We offer specialized expertise and extensive practical experience to assist client in developing management systems from the initial concept to establishment and successful implementation of the management systems.
We use the following consultation approach to assist you in achieving certification:
1. Identify areas requiring improvement or development within your current Management System
2. Prepare a strategic action plan, in conjunction with your company personnel, to address those improvement areas and assist with the communication of these requirements to key personnel at all levels
3. Provide system-related trainings for your company personnel to create awareness and provide them with the necessary knowledge and skills in the implementation of systems
4. Provide assistance and advice on the development and implementation of systems, including preparation of documentation
5. Advise and assist, if required, with the preparation and submission of applications to your certification body
6. Assist with the development of internal auditing procedures and training
7. Conduct internal audit to ensure the effective implementation of the management system prior to final audit by your certification body
8. Conduct Management Review Meeting to review performance of management system and identify areas for improvement prior to final audit by your certification body
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 ISO 13485:2016 MEDICAL DEVICES QUALITY MANAGEMENT SYSTEMSISO 13485:2016 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 standard is applicable to all manufacturers and providers of medical devices, components, contract services and distribution of medical devices.
Requirements of ISO 13485:2016
• Clause 4: Quality management system
• Clause 5: Management responsibility
• Clause 6: Resource management
• Clause 7: Product realization
• Clause 8: Measurement, analysis and improvement
Benefits of ISO 13485:2016
• Increase access to more markets worldwide
• Savings in cost from reduction of defects and rejects
• Meet relevant regulatory requirements and customer expectations
• Demonstrate ability to produce safer and more effective medical devices
• Improve operation efficiency through continual improvement processes
How can ELITE assist you?
ELITE provides ISO 13485 system training and consultancy services. We offer specialized expertise and extensive practical experience to assist client in developing management systems from the initial concept to establishment and successful implementation of the management systems.
We use the following consultation approach to assist you in achieving certification:
1. Identify areas requiring improvement or development within your current Management System
2. Prepare a strategic action plan, in conjunction with your company personnel, to address those improvement areas and assist with the communication of these requirements to key personnel at all levels
3. Provide system-related trainings for your company personnel to create awareness and provide them with the necessary knowledge and skills in the implementation of systems
4. Provide assistance and advice on the development and implementation of systems, including preparation of documentation
5. Advise and assist, if required, with the preparation and submission of applications to your certification body
6. Assist with the development of internal auditing procedures and training
7. Conduct internal audit to ensure the effective implementation of the management system prior to final audit by your certification body
8. Conduct Management Review Meeting to review performance of management system and identify areas for improvement prior to final audit by your certification body
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