FDA Drafts Guidance on Replacing Reagents for IVD Devices Post author:Sam Post published:February 15, 2018 Post category:The GMP Letter The FDA issued draft guidance to provide updates on in vitro diagnostics’ replacement reagents. Source: The GMP Letter You Might Also Like Cooperation, Not Confrontation, Key to Internal Audits April 7, 2017 FDA Accepts IEC Standards for Ultrasonic Diathermy Devices May 15, 2018 Perahealth Lacks Design Plans for Software June 4, 2020