EU Commission directive 2017/1569, GMP for investigational medicinal products for human use, 05/17 2021-09-17T13:52:09+00:00January 17th, 2020|
EU GMP Guide Part III, Guideline on setting health based exposure limits for use in risk identification in the manufacture of .., 06/15 2021-09-17T13:55:22+00:00January 17th, 2020|
21 CFR 205 Guidelines for state licensing of wholesale prescription drug distributors, 04/13 2021-09-17T13:23:40+00:00January 17th, 2020|
EU Compilation of Union Procedures on Inspections and Exchange of Information, Rev 18 Corr, 04/22 2022-09-07T04:17:17+00:00January 17th, 2020|
EU Commission directive 2001/83/EC, Community code relating to medicinal products for human use, 11/01 2020-07-29T12:13:35+00:00January 17th, 2020|