USP/EP Chapters

Master how to maintain compliance with evolving USP and EP chapters, and manage updates and revisions in your company’s quality systems.  

Explore microbiological testing as defined in USP and EP general chapters—learn how to ensure compliance in sterile and non-sterile product testing.  

Understand compendial testing methods for disintegration, dissolution, and spectrophotometry and their validation as per USP/EP requirements.  

Get familiar with the structure, purpose, and application of USP and EP monographs used globally for drug substance and drug product quality standards.