Module 19: Regulation of In Vitro Diagnostic Medical Devices

28/03/2023

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Team NB Position Paper

Best Practice Guidance for the Submission of Technical Documentation under Annex II and III of In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746

27 th February 2023

https://www.team-nb.org/team-nb-pp-best-practice-guidance-for-the submission-of-technical-documentation-under-annex-ii-and-iii-of-in-vitro diagnostic-medical-devices-regulation/

The Organisation for Professionals in Regulatory Affairs

17

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Best Practice Guidance for the Submission of Technical Documentation under Annex II and III f In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 27 th February 2023

The Organisation for Professionals in Regulatory Affairs

18