(DOWNLOAD) "Amendments to the Current Good Manufacturing Practice Regulations for Finished Pharmaceuticals (US Food and Drug Administration Regulation) (FDA) (2018 Edition)" by The Law Library " eBook PDF Kindle ePub Free
eBook details
- Title: Amendments to the Current Good Manufacturing Practice Regulations for Finished Pharmaceuticals (US Food and Drug Administration Regulation) (FDA) (2018 Edition)
- Author : The Law Library
- Release Date : January 06, 2018
- Genre: Law,Books,Professional & Technical,
- Pages : * pages
- Size : 196 KB
Description
The Law Library presents the complete text of the Amendments to the Current Good Manufacturing Practice Regulations for Finished Pharmaceuticals (US Food and Drug Administration Regulation) (FDA) (2018 Edition).
Updated as of May 29, 2018
The Food and Drug Administration (FDA) is amending certain of its regulations on current good manufacturing practice (CGMP) requirements for finished pharmaceuticals as the culmination of the first phase of an incremental approach to modifying the CGMP regulations for these products. This rule revises CGMP requirements primarily concerning aseptic processing, verification of performance of operations by a second individual, and the use of asbestos filters. We are amending the regulations to modernize or clarify some of the requirements as well as to harmonize them with other FDA regulations and international CGMP standards.
This ebook contains:
- The complete text of the Amendments to the Current Good Manufacturing Practice Regulations for Finished Pharmaceuticals (US Food and Drug Administration Regulation) (FDA) (2018 Edition)
- A dynamic table of content linking to each section
- A table of contents in introduction presenting a general overview of the structure