Dissolution Seminar Series: Dissolution Method; Design, Development and Validation
The Dissolution Method; Design, Development and Validation seminar is a comprehensive one-day course designed for pharmaceutical analysts with a practical working knowledge of dissolution as well as analysts developing, transferring and validating analytical methods. After an initial overview of the dissolution test the seminar will focus on the basics of dissolution method development, validation and transfer. Whether the participant is an experienced R&D or QC chemist involved in technology transfers, this seminar will provide detailed requirements for basic dissolution method development for biorelevant, discriminatory, rugged and validatable methods. While the course material focuses on solid oral dosage forms; the techniques and practices may be applied to other dosage forms. The essential components of method validation will be discussed with parameters and proposed acceptance criteria to maintain accurate, precise and reliable dissolution testing throughout the life of the pharmaceutical dosage form under development. Participants will be encouraged to share their method development experiences and participate in discussion.
Location: Agilent Technologies, 1 Yishun Ave 7
Date: March13, 2014
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