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UPCOMING WEBINARS

Clinical Payments Case Studies: Improving Efficiency, Cash Management, and Compliance

Sep-26

Lugano 2014 Criteria for Assessing FDG-PET/CT in Lymphoma: An Operational Approach for Clinical Trials

Sep-27

Development and Manufacture of Highly Potent API Drug Products Throughout the Clinical Phases

Sep-28

What Does it Take to Successfully Execute Large, Global, Phase III Programs?

Oct-3

Pharmacology to Payer: One Quantitative Drug Development Framework to Rule Them All

Oct-4

Biologics in Dermatology: Considerations for Patients and Clinical Trials

Oct-4

Why Track and Trace Isn’t Just Tracking and Tracing: Best Practices for Implementing a Solution That Works

Oct-4

Strategy Design & Formulation Considerations for GLP Toxicology Studies

Oct-5

NextGen Data Mapping Solutions for Better, Faster Compliance and Analytics

Oct-5

Pharma Competitive Intelligence: Delivering Actionable Insights for Decision Making

Oct-10

Electronic Informed Consent: 2017 Industry Survey Results from Clinical Sites

Oct-10

Beware the Hidden Costs of Conducting Clinical Trials: Understanding the Landmines and How to Avoid Them

Oct-11

Claims Substantiation – An Integrated Clinical and Regulatory Approach

Oct-11

Overcoming the Challenges of Conducting Clinical Studies in Rare Pediatric Populations

Oct-11

Food Safety: How Representative Sampling Can Reduce Your Risk

Oct-12

Linking Evidence and Value Strategies with the Right Stakeholder

Oct-13

Adaptive Trial Design and Incorporation of Biomarkers to Maximize Achievable Objectives in Early Phase Clinical Studies

Oct-13

 

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