RSS Newsfeed  Your shopping cart.
home
SEARCH

Search in

Keyword

Guideline

The following guideline can be ordered through the address listed in the "Source/Publisher"-category.
In cases in which you can order through the Internet we have established a hyperlink.

21 CFR Part 314.420 Drug Master Files
Short Title:21 CFR Part 314.420
Internet:http://www.gmp-compliance.org/guidemgr/files/CFR-2013-TITLE21-VOL5-SEC314-420.PDF
Origin/Publisher:FDA
Content:This part contains the FDA requirement for Drug Master Files in applications.
Document Type:Code of Federal Regulations

 GMP Conferences by Topics
 Quality Assurance
 GMP in Biotechnology
 Microbiology
 Regulatory Affairs
 GMP in Pharmaceutical Development
 Quality Control
 Storage, Distribution, Transportation
 Sterile / Aseptic Manufacturing
 Computer Validation
 Technical Operations
 GMP for APIs and Excipients
 Validation
 Medical Devices