Draft FDA Circular entitled “Specific List of Registrable In Vitro Diagnostic Medical Device (IVD) and Revised Technical Requirements for Registration of COVID-19 Test Kits
Draft FDA Circular entitled “Specific List of Registrable In Vitro Diagnostic Medical Device (IVD) and Revised Technical Requirements for Registration of COVID-19 Test Kits was issued on 11 February 2022.
- Agency
- Category