This webinar, presented by Olivier Barberan will offer insights, tools and best practice and will cover the following topics:

• How to leverage insights from precedent drugs to dramatically reduce costs and
decrease risk of delays in clinical trials
• How to optimize clinical trial design to reduce failure risk due to lack of efficacy
• How to mitigate the risk of doing unnecessary clinical trials by learning from past
regulatory feedback and quickly gaining information on similar and competitive drugs

The format of this webinar will be a 35 minute presentation followed by a Q&A session

Part of the PharmaPendium Webinar Series: Risk Assessment in Drug Development
Olivier Barberan
Director, Translational Medicine Solutions , Elsevier
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