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Marie Compagnon-Riobé, Regulatory Affairs Director at the Peters Surgical Group, explains in an article published in DeviceMed magazine the importance for manufacturers to involve the Regulatory Affairs and Quality Assurance (RAQA) department in the medical device design process.

Discover this article on pages 28 & 29 : https://www.devicemed.fr/magazine/devicemed-janvier-fevrier-2021/26058