EMA Process validation for the manufacture of biotechnology-dervied active substances, 04/16 2021-09-17T13:35:16+00:00November 20th, 2019|
FDA CPG Sec 460.800 Parametric Release – Terminally Heat Sterilized Drug Products, 10/87 2020-07-30T10:59:49+00:00November 20th, 2019|
FDA Guide to Inspections Validation of Cleaning Processes, 07/93 2019-11-20T11:01:54+00:00November 20th, 2019|
FDA Guide to Inspections of Oral Solid Dosage Forms Pre/Post Approval Issues for Development and Validation, 01/94 2020-02-18T11:13:30+00:00November 20th, 2019|
FDA GFI, for the Submission Documentation for Sterilization Process Validation in Applications…, 11/94 2021-09-22T13:03:19+00:00November 20th, 2019|