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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.
Recon | 12 October 2021 | By Kari Oakes
Tags: biologics, coronavirus, EMA, EU, FDA, IVDs, medical devices, oncology, pharmaceuticals, US