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Reagents for IVD Devices Post author:Sam Post published:February 15, 2018 Post category:The GMP Letter The FDA issued draft guidance to provide updates on in vitro diagnostics’ replacement reagents.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 Korean Facility Warned for Repeat Violations March 6, 2020 United Contact Lens Cited for Product Testing, Procedures January 18, 2017 EC Agrees on Common List of COVID-19 Rapid Antigen Tests March 4, 2021