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Detecting Potential Formulation Roadblocks in Early Drug Development

Moderator:

Rita Peters (Editorial Director, Pharmaceutical Technology, Pharmaceutical Technology Europe, and BioPharm International, UBM plc)

Panelists:

Ronald D. Snee, Ph.D. (Founder and President, Snee Associates, LLC)

Stephen Tindal (Director of Science Affairs, Catalent Pharma Solutions)

Location: 119A

Date: Tuesday, April 24

Time: 9:45am - 10:30am

Pass Type: Conference Pass, VIP Attendee - Get your pass now!

Track: Drug Development

Vault Recording: TBD

Catalent Pharma Solutions
Sponsor

Getting a compound to clinic is a milestone in the development of a drug. However, formulation hurdles or cost-prohibitive manufacturing challenges detected in later development stages can delay—or derail—the development and approval of a promising compound. Can the odds for getting a drug to market be improved by troubleshooting formulation challenges during early development phases? A panel of experts will review tools, strategies, and methods for assessing the formulation, drug delivery, and manufacturing potential of a drug candidate in preclinical phases. Implications for timelines, API materials, and budgets will be discussed.