Medical Devices, GDPMD

GDPMD is the Regulatory requirements for Medical Device Safety & Performance. In the Medical Devices Regulation 2012, Appendix 4 – Requirements on the Quality Management System, it specifies that Authorized Representative, Importer and Distributor is required to certify under GDPMD.


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Course Objective:

  • Understanding the GDPMD requirements
  • Awareness on the key elements to ensure medical device quality and safety along the supply chain.

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Course Objective:

  • Understanding of the GDPMD requirements
  • Understanding the audit principles
  • Plan, conduct, report and close out an internal audit
Duration: 1 day or 2 days Suitable for: This course is designed for those employees are appointed/potentially appointed as internal auditors, and those who would like to

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