How To Stop Good Pharmaceutical Formulations Going Bad
Selection of the appropriate techniques and assays, and their application in well-managed analytical programs, can simplify the process of deformulation and ensure a speedy route to market.
In this webinar, we’ll take a stepwise journey through the foundations of deformulation (reverse engineering) and in vitro bioequivalence (IVBE) testing, providing answers to these questions and more. We’ll consider challenges including the impact of flavor changes and container modifications on bioavailability profiles, and we’ll also take a deeper dive into the Q3 bioequivalence testing requirements for specific dosage forms.
Watch this webinar to find the answers to these commonly asked questions:
- What needs to be assayed?
- Which techniques should be applied?
- What should our testing program look like?