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Academic Medical Centers and Clinical Research Productivity: How to Choose The Best Sites $249.00 Anita Kablinger		Adapting Project Risk Mitigation and Prevention Tools in Real-Life Trials $199.00 Susan Schenk		Adaptive Clinical Trials: How Advanced Adaptive Methods Can Improve Your Next Study $249.00 Michael Rosenberg
Adaptive Trial Design: Streamlining the Clinical Supply Process $249.00 Geert Langendries		An Overview of Recent Risk-based Monitoring Guidance from the FDA $249.00 Joy Frestedt		Benefits & Risks Throughout the Product Lifecycle: How to Strike a Balance in a Post-FDAAA World $249.00 Edgar Adams & Robin Carter
Best Practices for Back Translation as a QA Tool $249.00 Hilary Davies		Best Practices for Writing Safety Narratives $249.00 Susan Sisk		Beyond Global Feasibility: An Evidence-Based Approach to Creating Realistic Development Timelines $249.00 Kent Thoelke
Choosing and Managing Contract Medical Writers $249.00 Susan Sisk		Clinical Data Capture Standards for Regulatory Submission Trials $249.00 Kit Howard		Clinical Investigations in Asia $249.00 Edward Ian
Clinical Trial Insurance and Indemnification Issues $249.00 Julia Johnson		Clinical Trial Success in Latin America $249.00 Federico Lerner		Clinical Trial Supply Challenges in China, Russia, Brazil & the Ukraine $249.00 Karen Oliver & Tracci Gilchrist

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