QA/RA Consultant
MedQAIR
Seasoned Quality and Regulatory Affairs Consultant. Main experience in the field of Software Medical Devices and Artificial Intelligence. In-depth knowledge and understanding of the EU and US regulatory frameworks, and specifically regarding quality, regulatory and information security. Further member of the SC 42, JTC 21 and TC 62 standardisation committees.
Disclosure information not submitted.
The Interface of the EU AI Act and the MDR/IVDR
Wednesday, October 23, 2024
11:45 AM - 12:45 PM CEST