108 Questions & Answers on MDR

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Written by the longest serving lawyer at the medical devices unit of the European Commission, this publication covers and addresses in the same place 108 practical questions and answers about the MDR, ranging from general questions, to questions to product qualification, general safety, conformity assessment, procedural aspects, manufacturer’s liability and clinical evaluation. Read 108 Questions & Answers and come to the legally safest side!

Verify the quality of the publication by downloading its free version:108 Questions & Answers – Safety Collection