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Periodic Safety Update Report for medical devices : A Concise Guide
Understand when and how to effectively write a PSUR for your medical devices according to European Regulation (EU) 2017/745.
Tristan GICQUEL
Apr 30, 20244 min read
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Classification of Medical devices in Europe: A Concise Guide
Understanding the nuances of the classification of medical devices according to European regulation is a crucial step for biotechnology...
Tristan GICQUEL
Apr 2, 20244 min read
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MEDICAL DEVICE R&D - International Regulatory Aspects
INTRODUCTION "I invite you to explore the primary challenges and opportunities in research and development (R&D) within the medical...
Tristan GICQUEL
Feb 13, 20246 min read
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