Free Whitepaper: How to Create Valuable Testing Data to Optimize Your Semisolid Formula Using In Vitro Release Testing Methodologies
Our unique In Vitro Release Testing (IVRT) expertise can assist you with:
- In process testing for formulation optimization
- Quality Control for lot-to-lot variability
- In Vitro and analytical method development and validation in full compliance with FDA SUPAC-SS guidelines
- In Vitro Release Rate comparison testing for pre and post-change formulations
- In Vitro Release Rate testing for manufacturing site transfer
- Skin Penetration Studies for Bioequivalency and Bioavailability evaluations
- Data interpretation and FDA submission for approval of SUPAC-SS related changes
By utilizing these methodologies, learn how you can avoid costly clinical studies and develop a better drug product.