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Upcoming Audio Conferences

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Achieving Global Registration of Complex Biosimilars		An Integrated Approach to Managing Supply Chain Risk		Current FDA Thinking on Risk Evaluation and Mitigation Strategies
Electronic Informed Consent: Putting the Pieces Together for Implementation		Electronic vs. Paper Data Capture: Which Option is Best for Your Trial?		Establishing Value for Diagnostics & Biomarkers in a Real-Life Setting
EU Centralized Procedure for Generics		Finding and Assessing Global Drug Development Partners		Generating High Performance: Beyond Technical Abilities
Japanese Medical Device Submission Requirements & Structure		Outsourcing and Offshoring in a New Era of FDA Enforcement		Points to Consider when Presenting Documents for an FDA Inspection
Quality Testing for Complex Medical Devices		The 2010 MDD Revisions and What They Mean for Translation

Adaptive/Novel Designs in Oncology: Overview & Issues
SKU: ac20090519

Design and Regulatory Considerations in Anti-Infective Drug Development
SKU: ac20091216

An Overview of EMEA & Centralized Procedure
SKU: ac20080624