Understanding The 5 Elements Of cGMP


Current Good Manufacturing Processes (cGMP) are outlined by the FDA, which defines them as the “minimum requirements for the methods, facilities, and controls used in manufacturing, processing, and packing of a drug product.”

Together, cGMPs help ensure consumers get a product that’s safe to use, and that it has the ingredients, strength, and other elements that it claims to have.

At Andelyn Biosciences, we always follow all cGMPs required by the FDA to maintain product safety, so let’s discuss the basic elements of cGMP, also known as the or “5 Ps” of CGMP.

The 5 Ps Of CGMP – What You Should Know

access the Article!

Get unlimited access to:

Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue. X

Enter your credentials below to log in. Not yet a member of Cell & Gene? Subscribe today.

Subscribe to Cell & Gene X

Please enter your email address and create a password to access the full content, Or log in to your account to continue.


Subscribe to Cell & Gene