Demos / Webinars
Life Sciences Webinar Series
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The Right eTMF Approach for You: Sponsor or CRO-Owned eTMF?
June 18, 2019
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Rethinking Medical Device go-to-market clinical strategies in the light of the new European MDR
May 2, 2019
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Content Requirements Under MDR…And What You Can Do About It
June 27, 2019
-- Past Webinars - This Page Requires Registration Before Viewing Content --
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eTMF + IRB Integration = Efficiency
March 31, 2016
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Best Practices for Achieving TMF Quality
June 10, 2015
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Translation of eCOA in Global Studies - Challenges and Solutions
December 20, 2014
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Clear & Simple: Reduce Content Costs with Global English
September 22, 2013
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Year One: The Pharmacovigilance System Master File
June 5, 2013
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Optimizing Sponsor / Provider Relationships by using Lessons Learned
June 14, 2011
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A Practical Guide to Patents for Scientists: Understanding Patents as a Source of Information in Research and Development
March 18, 2011
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Optimizing Country Selection in Oncology Clinical Trials
October 27, 2010
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Pharmacovigilance - How to Do More with Less
October 13, 2010
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Health Technology Assessment (HTA) in the Latin American Region Observations on Recent Trends
April 13, 2010
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Creating Value through the Application of Health Technologies in Clinical Trials
April 7, 2010
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Lessons Learned: Implementation of Electronic Submissions
March 17, 2010
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System Dynamics and Modeling - A Disease Management Technology Strategy Proof of Principle
February 10, 2010
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An Atlas for India
November 4, 2009
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The Culture of Drug Development in Japan
October 7, 2009
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E-Learning Strategies for a Global Audience
September 9, 2009
