Kirsten Van Garsse, Authorized Representative Director & Regulatory Affairs Manager
Regulatory Affairs
In Vitro Diagnostics
Medical Devices
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On October 7th, 2024, the Medical Device Coordination Group (MDCG) released a new guidance and templates for the assessment of Corrective and Preventive Action (CAPA) plans, intended for conformity assessment bodies, notified bodies, designating authorities, and Joint Assessment Teams involved in the implementation of Regulation (EU) 2017/745 (MDR) and Regulation (EU) 2017/746 (IVDR).
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