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This comprehensive resource covers product change evaluation, postmarket surveillance, audit/inspection compliance, and various other laws and regulations pertaining to maintaining a product on the market.
Hear from leaders around the globe as they share insights about their experiences and lessons learned throughout their certification journey.
Seyed Khorashahi, MSc, and Mark Agostino, MSc
Feature Articles | 25 May 2021 | Citation
Tags: lifecycle, MDR, medical device, Medical Device Regulation, postmarket surveillance, UDI