FDA GFI, Generally Accepted Scientific Knowledge in Applications for Drug and Biological Products: Nonclinical Information, DRAFT, 05/23 Anastasija Eschricht2023-06-27T09:47:42+00:00June 27th, 2023|
OECD Advisory Document: Quality Assurance and GLP, DRAFT, 09/21 Anastasija Eschricht2023-03-21T12:49:52+00:00March 21st, 2023|
ICH Guideline Viral Safety evaluation Biotech products derived from cell lines of human or animal origin, Q5A(R2), 09/22 Anastasija Eschricht2022-12-07T10:16:18+00:00December 7th, 2022|
EMA Guideline Plastic primary packaging materials, 05/05 Anastasija Eschricht2022-12-07T09:55:38+00:00December 7th, 2022|
OECD Number 17 Application of GLP Principles to Computerised systems, 04/16 Beatrice Burtsov2022-11-09T09:45:08+00:00November 9th, 2022|
ICH Guideline, Guideline for Elemental Impurities, Q3D(R2), 04/22 Beatrice Burtsov2022-11-09T08:56:55+00:00November 9th, 2022|
