Stability Evaluation and Retest Dating of Clinical Trial Materials (Investigational Medicinal Products)
Recorded Date: August 2004
Course Type: Recorded On-line Seminar
Speaker:
Carol Fowler, Asst. Senior Pharm Chemist, Eli Lilly & Co.
Do you need timely and useful information to improve your clinical trial material stability program and retest dating process? This Recorded On-line Seminar covers various approaches to the stability testing and retest dating of clinical trial materials. It discusses stability study designs and requirements. This On-line Seminar also covers how the stability data generated are translated into retest dates and subsequent dating extensions for clinical trial material.
At the end of this Recorded On-line Seminar, delegates are able to determine what stability studies are needed to support the clinical trial program, evaluate stability data to determine appropriate retest dating periods for clinical trial materials, and understand current regulatory requirements for clinical trial material stability and retest dating.
Who Should Attend
This Recorded On-line Seminar benefits development personnel, e.g., stability scientists, clinical trial material associates, analytical chemists, and anyone responsible for the development of stability programs and interpretation of stability data for clinical trial materials.
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