Drug Dissolution of Biopharmaceutical Products

Disintegration has become an important and broadly used test receiving more accentuation worldwide from regulatory specialists amid the last 15 years. It is a critical quality control excessively and a guide, making it impossible to formulation development. Dissolution testing measures change on stability, and is utilized to build up in-vitro in-vivo correlations for some products. The disintegration test has experienced changes and updates subsequently of the expanded regulatory interest and the pharm practical industry's examination of aspects of disintegration testing to additionally enhance and get it the technique.

  • Diffusion Layer Model
  • The Interfacial Barrier Model
  • Modelling Random Effects
  • Comparison of Dissolution Profiles

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