EMA Guideline on the sterilisation of medicinal product, active substance, excipient and primary container, 03/19 Lars-Eric Ellow2023-06-09T07:21:08+00:00December 10th, 2019|
EU GMP Guide Part IV – Guidelines on Good Manufacturing Practice specific to Advanced Therapy Medicinal Products, 11/17 2021-09-17T13:57:20+00:00November 20th, 2019|
FDA GFI, Validation of Procedures for Processing of Human Tissues Intended for Transplantation, 03/02 2021-09-22T14:00:37+00:00November 20th, 2019|
21 CFR 1271 Human cells, Tissues, and Cellular and tissue-based products, 08/17 2021-09-17T13:22:36+00:00November 20th, 2019|