FDA 21 CFR 211: cGMP for Finished Pharmaceuticals * Free *

Date Published:
Thu, 04/01/2010

FDA federal regulation for the manufacturing of finished pharmaceutical drug products.  Sections most frequently applied to software include:

  • 68 (a) and (b):  Automatic, mechanical, and electronic equipment
  • 160 (b): General requirements; lab controls
  • 194 (a): Laboratory records