Why Should You Attend:
Drug development has a poor track record, with only about 1 in 10 clinical development candidates making it to approval, and with 50% of drugs in Phase 3 trials testing no different from placebo. At the same time, acceptability of regulatory submissions demands improvement, with a recent dramatic increase in NDA filings rejected without review on grounds of insufficient quality. Over the past decade, the FDA has worked with the pharmaceutical and biotech industries to devise a way to improve both the quality of regulatory new drug submissions as well as the success rate of drug development. One outcome of this collaboration is the FDA Guidance on End-of-Phase 2A meetings.
This webinar will describe how drug developers can use the FDA end-of-phase 2A meeting to facilitate development through better decisions and regulatory acceleration while improving compliance with FDA Guidelines and expectations.
Areas Covered in the Webinar:
Who Will Benefit:
Roger D. Toothaker, is the founder of PKPD Strategies, LLC, a New Jersey-based consulting organization dedicated to improving the quality and successfulness of drug development and regulatory submission activities. Mr. Toothaker has over 30 years of nonclinical and clinical drug development experience with both small molecules and biologics across all major therapeutic indications, and has held positions in industrial, contract, and academic settings. He received his PhD in Pharmaceutics from the University of Wisconsin, and is a member of AAPS, ASCPT, and AAAS.
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