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MD-QMS Comprehensive EU Medical Device Regulation 2017/745 (EU MDR) Practitioner (Medical Device – Quality Management System)

This course aims to provide learners who have an existing, basic knowledge of, or experience in, quality management in the Medical Device Industry with an in-depth understanding of the application under the European Union’s Medical Device Regulation (EU-MDR 2017/745) Regulation.

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MD-SAP Auditing Approach (Medical Device – Single Audit Program)

This course aims to provide learners with the knowledge and skills required to understand and complete an audit against the IMDRF Medical Device Single Audit Program (MDSAP AU P0002.005) for medical device quality management.

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MD-QMS ISO 13485:2016 Internal Auditor (Medical Device – Quality Management System)

This course provides learners with the knowledge and skills to perform an internal audit of part of a quality management system based on ISO 13485. and applicable international regulatory standards report on the effective implementation and maintenance of the management system.

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ISO 50001:2018 Internal Auditor (EnMS)

This course provides delegates with the knowledge and skills required to perform an internal audit of part of an energy management system based on ISO 50001 and report on the effective implementation and maintenance of the management system in accordance with ISO 19011.

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ISO 22000:2018 Internal Auditor (FSMS)

This course provides delegates with the knowledge and skills required to perform an internal audit of part of a food safety management system based on ISO 22000 and report on the effective implementation and maintenance of the management system in accordance with ISO 19011.

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ISO 22000:2018 auditor transition training (FSMS)

ISO 22000:2018 is now the new standard for Food Safety Management Systems. The deadline to transition to this standard passed on 31 December 2021. However, we understand that some auditors may not have had a business need to transition by the deadline.

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