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MichBio U: Drug Development Regulations
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Learn some basic information regarding key decisions and challenges faced during early drug development and the approaches to develop an effective early strategy.

5/27/2014
When: 5/27/2014
10-11 a.m.
Where: Webinar
Contact: MichBio U
734.527.9150


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Regulatory Overview of Early Drug Development Webinar

 

Early drug development is a key time in the life of a potential new drug. Decisions and strategy employed at this early stage can affect later development and even registration of a new product. 

In this webinar Ross Lobell, Principal Consultant at RegSource Consulting Inc., will present some basic information regarding key decisions and challenges faced during early development and approaches to develop an effective early strategy. In addition, he will show how regulatory professionals can be an important ally in arriving at the best strategy for a given molecule. It is hoped that the listener will gain an appreciation for some of the complexities of the strategic process that is relevant to modern drug development for both small and large molecules.

 

Lobell has been in the pharma/biopharma business for over 30 years having worked at Schering-Plough, Pfizer, Amgen and most recently MedImmune/Astra-Zeneca. He has had regulatory responsibilities for a variety of therapeutic areas including oncology, pulmonary, auto-immunity, lipid metabolism, and virology and has participated in drug development throughout all stages, including NDA/BLA submissions.

 

MichBio U is generously supported by Bank of America Merrill Lynch.
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