Introduction to CFRs 210 & 211 for Finished Pharmaceuticals

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cfrs fda

This interactive e-Learning course provides personnel with the key concepts in CFRs Part 210: Current Good Manufacturing Practice in Manufacturing, Processing, Packing or Holding of Drugs; General, and Part 211: cGMP for Finished Pharmaceutical.

The course is linked to the 2015 top 10 FDA warning letter findings and will assist new QA and supervisory personnel navigate these lengthy regulations.