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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.
RAPS' Latest | 23 August 2018 | By Zachary Brousseau
Tags: book, device, devices, medical, process, publication, Sherman, validation, verification