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ISO 37001:2016 Anti-bribery Management Systems

ISO 37001:2016 Anti-bribery Management Systems

ISO 37001 is an anti-bribery management systems standard published in October 2016.  It is designed to help an organization establish, implement, maintain, and improve an anti-bribery compliance programme.  It includes a series of measures and controls that represent global anti-bribery good practice.
ISO 37001 is based on a four-step model and aligned with the ISO 19600 standard for Compliance Management Systems:

  • Plan: identify anti-bribery obligations and evaluate compliance risks in order to develop a strategy, including measures to address any issues

  • Do: implement measures and establish mechanisms to monitor their effectiveness

  • Check: review the anti-bribery management program on the basis of the controls implemented

  • Act: review and improve the program continually, ensuring cases of noncompliance are monitored and examined

 

Requirements of ISO 37001:2016

The organization must implement a series of measures and controls in a reasonable and proportionate manner to help prevent, detect, and deal with bribery, including:

  • Anti-bribery policy

  • Management leadership, commitment and responsibility

  • Personnel controls and training

  • Risk assessments

  • Due diligence on projects and business associates

  • Financial, commercial and contractual controls

  • Reporting, monitoring, investigation and review

  • ​Corrective action and continual improvement
     

Benefits of ISO 37001:2016

  • Assists a company in implementing an anti-bribery management systems, or in enhancing its existing controls, with the potential to reduce corporate risk and costs related to bribery.

  • Helps provide assurance to the management and owners of a company, and to its funders, customers and other business associates, that the company has implemented internationally recognized good practice anti-bribery controls. 

  • Helps in the event of an investigation to provide evidence to the prosecutors or courts that the company had taken reasonable steps to prevent bribery

 

How can ELITE assist you?

We provide ISO 37001 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
 

GDPMD (Good Distribution Practice for Medical Devices)

With the effective date (1 July 2013) of Act 737 and Medical Device Regulations 2012, manufacturers and distributors of medical devices are required to apply for their establishment licence to continue carrying out their manufacturing, distribution or importing activities.
Manufacturers require ISO13485 Medical Devices Quality Management System certification whereas Distributors, Importers and local Authorized Representative require Good Distribution Practice for Medical Devices (GDPMD) certification prior to applying for their Establishment Licence.
 

GDPMD requirements consists of 6 parts:

1. Preliminary
2. Organization and GDPMD Regulatory Compliance System
3. Establishment Responsibilities
4. Resource Management
5. Supply Chain and Device Specific
6. Surveillance and Vigilance
 

Benefits of GDPMD

Savings in cost from reduction of defects and rejects
Meet regulatory requirements and customer expectations
Consistency to proper storage, handling, distribution and traceability
Demonstrate ability to produce safer and more effective medical devices
Improve operation efficiency through continual improvement processes
 

How can ELITE assist you?

ELITE provides GDPMD 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
 

ISO Training Courses

2-Day ISO9001/14001 Awareness & Application 
 
2-Day Internal Audit Course ISO 9001 
 
2-Day Internal Audit Course ISO 14001 

2-Day Internal Audit Course ISO 45001
 
2-Day Internal Audit Course ISO 22000

Management Representative (MR) Training

Risks Management Training

KPI Training
 
All Systems Assured courses are based at your office - you don’t pay for travel costs
 
Each delegate receives a certificate The course tutors are all IRQA working systems consultants with considerable experience in the implementation and auditing of each subject matter. 

IATF 16949:2016 Automotive Quality Management Systems

IATF 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
 
 

ISO/IEC 17025:2017 General Requirements for the competence of testing and calibration laboratories

ISO/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. 
ISO/IEC 17025 is applicable to all organizations performing laboratory activities, regardless of the number of personnel.
 

Requirements of ISO/IEC 17025

• Clause 4 General requirements
• Clause 5 Structural requirements
• Clause 6 Resource requirements
• Clause 7 Process requirements
• Clause 8 Management system 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.
• Helps facilitate cooperation between laboratories and other bodies by generating wider acceptance of results between countries.
• Test reports and certificates can be accepted from one country to another without the need for further testing, which, in turn, improves international trade

 

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.
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


 




 

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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