USP Workshop: Value of Pharmacopeial Standards

The purpose of these workshops are to share an overview of how Pharmacopeial Standards can help fostering innovation and market access for supply of quality medicines. We will share effective use of USP documentary and reference standards and explain the development of Pharmacopeial Reference Standard.

Overall USP’s perspectives and resources will also be discussed including information on USP’s General Chapters, Reference Standards and Pharmaceutical Analytical Impurities (PAIs) which are designed to support manufacturers in monitoring and controlling the level of impurities in their products will be shared as well.

Agenda:

• Effective use of USP documentary and reference standards
• Development of Pharmacopeial Reference Standard and understanding uncertainty
• Discussion of USP Impurity relevant general chapters, including Nitrosamines

Why attend:

• Learn how Pharmacopeial Standards Ensure the Quality of Medicines
• Discover USP’s approach to impurities in drug substances and products
• Stay updated on USP standards and resources for impurities control
• Participate in Q&A sessions with USP representative

Click on the location below to register: