EMA Guidance for individual labs for transfer of QC methods validated in collaborative trials, view to implementing 3Rs, 11/17 2019-11-20T11:14:00+00:00November 20th, 2019|
FDA GFI, Heparin-Containing Medical Devices and Combination Products: Recommendations for Labeling and Safety Test, 09/18 2021-09-22T13:09:58+00:00November 20th, 2019|
FDA GFI, Elemental Impurities in Drug Products 06/16 DRAFT 2021-09-22T12:52:57+00:00November 20th, 2019|
FDA GFI, Validation of Growth-Based Rapid Microbiological Methods for Sterility Testing of Cellular and Gene Therapy Prod, 02/08 DRAFT 2021-09-22T14:00:05+00:00November 20th, 2019|
FDA GFI, Analytical Procedures and Methods Validation for Drugs and Biologics, 07/15 2020-02-17T14:04:26+00:00November 20th, 2019|