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When you need on-site attention, we’re not just here to help, we’re there to help—right by your side.
Individual courses are remarkably effective. But sometimes when you have a specific need, it helps to have expert guidance right in the room with you and your team.
In that case, we’re happy to design a custom training for your entire team, whether online—or on-site.
Learn moreRemember – at checkout you can choose to take this course On-demand. We offer a 10% group discount when you register 2 of more attendees (up to 10). Contact us for larger groups.
“An Intensive Review of Technical and Regulatory Aspects
No drug product enters the marketplace without adequate stability data first. While ICH has harmonized and standardized the approach to performing stability, a number of challenges are still routinely faced while conducting stability testing. Since inadequate stability can lead to product introduction delays, all drug companies need to ensure their programs are acceptable.
This 18-hour accredited training course focuses on the science and principles concerning stability of pharmaceutical, biotechnology and cosmetic products. Kinetic approaches to chemical stability will be covered and the advantages and limitations of accelerated stability testing will be discussed. Degradation by chemical, physical and microbiological factors will be covered. Data analysis and practical aspects of stability such as the role of packaging in stability will be included. Considerable attention will be given to analytical methodology, data analysis and data management. Current FDA Stability guidelines and ICH Guidelines on stability will be discussed.
The course includes a workshop for hands-on experience of data and statistical analysis.
Can’t Make the LIVE Course dates?
You can register now for the on demand! Simply select the On Demand option when registering and we will automatically send you access to the recorded version for you to view for 30 days. On Demand will be available within 2 weeks after the live offering.
PLEASE NOTE: Since this training is highly interactive, you must have a webcam on your computer equipped with a microphone and speakers/headset in order to fully participate.”
This course contains in-depth coverage of the science and practice of drug stability, shelf-life and is designed to benefit the following personnel:
– QC/QA Managers/Supervisors
– Product Stability Managers
– Manufacturing Personnel
– Research & Product Development Scientists and Managers
– Regulatory Personnel
– Pharmaceutical Consultants
Personnel who routinely review stability data or reports would additionally benefit from this course by gaining a broader understanding of stability testing.
Dr. Pardeep K. Gupta
Professor of Pharmaceutics, Philadelphia College of Pharmacy, University of The Sciences in Philadelphia (USciences)
Dr. Pardeep K. Gupta is a Professor of Pharmaceutics in Philadelphia College of Pharmacy at the University of The Sciences in Philadelphia (USciences). He received his B. Pharm. and M. Pharm. (pharmaceutical chemistry) degrees from India. He also received a M.S. degree in medicinal chemistry from USciences and his Ph.D. in pharmaceutics from University of Wisconsin. His research interests include delivery of proteins and peptides and study of the interaction of drugs with biomembranes. He has published several articles and has authored several book chapters. His teaching responsibilities include courses in solubility, controlled drug delivery and drug stability at the graduate level. He is on the editorial board of Remington: The Science and Practice of Pharmacy, and is the editor of Pharmaceutical Chemistry and Pharmaceutical Testing, Analysis and Control sections of the book.