ISO 9001: 2015 | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
ISO 9001:2015 sets out the criteria for a quality management system and certification. It can be used by any organization, large or small, regardless of its field of activity. In fact ISO 9001:2015 is implemented by over one million companies and organizations in over 170 countries. This standard is based on a number of quality management principles including a strong customer focus, the motivation and implication of top management, the process approach and continual improvement. Using ISO 9001:2015 helps ensure that customers get consistent, good quality products and services, which in turn brings many business benefits |
ISO 14001:2015 | ||
Std requirements 1 Day | Internal auditing 2 Days | Lead Auditing 5 days |
ISO 14001:2015 is applicable to any organization that wishes to establish, implement, maintain and improve an environmental management system, to assure itself of conformity with its stated environmental policy, and to demonstrate conformity with legal requirements and other requirements to which the organization subscribes, and information about significant environmental aspects |
OHSAS 18001:2007 | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
OHSAS 18001 is an Occupation Health and Safety Assessment Series for health and safety management systems. It is intended to help an organizations to control occupational health and safety risks. It was developed in response to widespread demand for a recognized standard against which to be certified and assessed. |
ISO 13485: 2003 | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
The primary objective of ISO 13485:2003 is to facilitate harmonized medical device regulatory requirements for quality management systems. 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. All requirements of ISO 13485:2003 are specific to organizations providing medical devices, regardless of the type or size of the organization. |
ISO 22000:2005 | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
ISO 22000:2005 sets out the requirements for a food safety management system and can be certified to. It maps out what an organization needs to do to demonstrate its ability to control food safety hazards in order to ensure that food is safe. It can be used by any organization regardless of its size or position in the food chain. |
ISO 17025 :2005 | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
ISO/IEC 17025:2005 is for use by laboratories in developing their management system for quality, administrative and technical operations. Laboratory customers, regulatory authorities and accreditation bodies may also use it in confirming or recognizing the competence of laboratories. ISO/IEC 17025:2005 is not intended to be used as the basis for certification of laboratories. It is applicable to all organizations performing tests and/or calibrations. These include, for example, first-, second- and third-party laboratories, and laboratories where testing and/or calibration forms part of inspection and product certification. |
ISO 15189 :2012 | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
ISO 15189:2012 can be used by medical laboratories in developing their quality management systems and assessing their own competence. It can also be used for confirming or recognizing the competence of medical laboratories by laboratory customers, regulating authorities and accreditation bodies. |
ISO 27001: 2013 ` | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
The ISO 27000 :2013 family of standards helps organizations keep information assets secure. ISO/IEC 27001 is the best-known standard in the family providing requirements for an information security management system (ISMS) ,helps organizations keep information assets secure within the context of the organization’s overall business risks I is designed to ensure the selection of adequate and proportionate security controls that protect information assets and give confidence to interested parties. |
ISO 31000 :2009 | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
ISO 31000:2009 provides generic guidelines for the design, implementation and maintenance of risk management processes throughout an organization. This approach to formalizing risk management practices will facilitate broader adoption by companies who require an enterprise risk management standard that accommodates multiple ‘silo-centric’ management systems. The scope of this approach to risk management is to enable all strategic, management and operational tasks of an organization throughout projects, functions, and processes to be aligned to a common set of risk management objectives. |
ISO 50001: 2011 | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
The main objective of the standard is to improve energy-related performance and energy efficiency continuously and to identify energy reduction opportunities. This systematic approach will help organizations to establish systems and processes. |
ISO /TS 16449:2007 | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
The standard is applicable to any organisation that manufactures components, assemblies and parts for supply to the automotive industry covering fabricating production materials, production or service parts, assemblies or heat treatment, welding, painting, plating or other finishing services. |
Lean Six Sigma | ||
3 days in line with live workshops and projects. Lean Six Sigma emphasizes the use of Lean methodologies and tools to identify and remove waste and increase process velocity, then follows that with the use of Six Sigma methodologies and tools to identify and reduce or remove process variation. |
Six Sigma Green Belt. | ||
3 days in line with live workshops and projects. Six Sigma Green Belt training provides participants with enhanced problem-solving skills, with an emphasis on the DMAIC (Define, Measure, Analyze, Improve and Control) model. Six Sigma Green Belt certification helps the employee serve as a trained team member within his or her function-specific area of the organization. This focus allows the Green Belt to work on small, carefully defined Six Sigma projects, requiring less than a Black Belt’s full-time commitment to Six Sigma throughout the organization. |
Six Sigma Black Belt | ||
15 days in line with live workshops and projects. A Six Sigma black belt is a specialist who saves the company money. The job of the black belt consists of analyzing business and operations processes and suggesting and implementing more efficient ways of performing functions, which in turn will hopefully save the company money. A person who has a black belt certification is usually highly sought after by any company looking to improve its bottom line. |
CE Marking | ||
Std requirements 1 Day | Internal auditing 2 Day | Lead Auditing 5 days |
CE marking is mandatory for certain product groups within the European Economic Area plus Switzerland and Turkey. The manufacturer of products made within the EEA and the importer of goods made in other countries must ensure that CE-marked goods conform to standards. |