Скачать или смотреть Dissolution Testing for Orally Administered Dosage Forms

Dissolution testing is a critical step in pharmaceutical development and quality control. It measures the rate and extent to which the active drug ingredient is released from an oral dosage form—such as tablets, capsules, or suspensions—into solution, making it available for absorption in the body.

In this video, we’ll cover:
✅ The purpose and importance of dissolution testing
✅ Methods and apparatus used in dissolution studies
✅ Factors affecting dissolution rate
✅ Regulatory perspectives and pharmacopeial guidelines
✅ Applications in formulation development, bioequivalence studies, and product quality assurance

Whether you are a pharmacy student, researcher, or industry professional, this video will help you understand why dissolution testing is considered one of the most vital quality control tools in pharmaceuticals.