The University of Texas at Austin College of Pharmacy welcomes a new collaboration with The National Institute for Pharmaceutical Technology and Education (NIPTE).
The University of Texas at Austin College of Pharmacy Division of Pharmaceutics and the distinguished members of the Planning Committee welcome you to the Annual International Conference on Drug Development (ICD2).
ICD2 continues its tradition of offering an informal forum for the exchange of ideas concerning the drug discovery and drug development process.
Offering the Most Informative and Up to Date Information in the Science and Regulation of Global Drug Development
Target Audience
REGULATORY • PHARMACEUTICAL & BIOTECHNOLOGY INDUSTRY • ACADEMIA
This conference is intended for leaders in Academia, the Pharmaceutical and Biotechnology Industry (PhRMA, BIO, GPhA), contract research organizations, API manufacturers, and domestic and international regulatory agencies in positions to affect the science and regulation of drug discovery and development, who wish to stay abreast on the national and international initiatives affecting the development of safe and effective pharmaceutical drug products.
Why Attend ICD2?
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“I do not understand why anyone who works in regulatory affairs in drug development is not at this meeting.”
Gerald J. Yakatan, Ph.D. Founder & Chairman, IriSys, Inc. |
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“The tremendous strengths of the ICD2 is the fact that you have top people from the FDA, top people from industry, top people from other organizations, the legal groups, academic institutions all getting together and really trying to hash out some of the major challenges that the industry and the environment is dealing with and find ways to move forward.”
Kenneth I. Kaitin, Ph.D. Professor and Director • Tufts Center for the Study of Drug Development, Tufts University |
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“The ICD2 is an incredibly intimate setting which allows dialogue on cutting edge topics with not only senior scientists and policy makers at the FDA, but academicians and other senior scientists and executives from industry, the opportunity to exchange that dialogue and discuss those topics in not only a small, intimate conference setting, but also over three meals a day, is really a unique opportunity. It’s not a typical conference.”
Joanne Palmisano, M.D., FACP Vice President, Drug Regulatory Affairs • Boehringer Ingelheim Pharmaceuticals, Inc. |
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“This is an unparalleled, not-to-be-missed opportunity to network with industry colleagues who are at the cutting edge of drug development and regulation, academics and legal wizards who establish and illuminate regulatory policy, and senior FDA officials. ”
Kay Holcombe Senior Vice President for Science Policy • Biotechnology Innovation Organization (BIO)Administration |
