‘Topical Dermatological Product Development in the USA’ Workshop to Be Held on June 4, 2009 in East Brunswick, New Jersey, USA
Featuring US experts in topical dermatological drug development
This workshop will focus on the unique problems and issues confronted during development of topical dermatological drugs intended for the US market.
“Our line-up of dermatological experts for this workshop is exceptional,” said
The morning session will cover formulation and screening of topical products for regulatory, clinical and commercial success, CMC issues and pitfalls, and the role of project management in successful development programs.
The afternoon session will cover FDA safety concerns and non-clinical requirements, clinical endpoints and trial designs. The FDA perspective will be presented by the retired founding director of the FDA Dermatology Division, including strategies for successful FDA meetings.
A Q&A roundtable to include all speakers will conclude the program.
A reception from
See www.dowpharmsci.com for information on this exciting workshop.
Contact:
Vanlee Waters, Dow Pharmaceutical Sciences at 707.796.7239
E-mail: vwaters@dowpharmsci.com
SOURCE Dow Pharmaceutical Sciences, Inc.
