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Registration fees

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Non-Member Price

$2029

Member price:

$1799

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#42: Patient Preferences: Using Conjoint Analysis and Stated Preferences in Drug Development and Regulatory Decision Making

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#41: Toolkit Approach to Best Practices in Root Cause Analysis and CAPA Management Workshop

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#43: Back to the Future: Combination Products in the 21st Century

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#20: Real World Evidence Studies to Evaluate the Safety and Effectiveness of Therapeutic Interventions – Is the Data Fit for Purpose and How Will You Know?

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#21: Basics of European Medical Device Regulation

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#22: Protocol Co-Design with Patients and Advocates

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#23: Preparing for a US FDA Advisory Committee Meeting

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#24: Data Visualization in the Life Sciences

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#27: eCOA 101: The What, Why, and How of eCOA to Reduce Barriers to Adoption in Clinical Studies

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#30: Machine Learning in Pharmacovigilance

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#33: European Regulatory Meetings: How Best to Prepare and Perform

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#34: Implementing a Risk-Based Monitoring Solution: Understanding the Basics of a Sustainable Model

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#35: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Effecting Pharmaceutical Development

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#36: A Novel Interactive Safety Graphic to Evaluate Potential Drug-Induced Hepatotoxicity

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#37: Patient Literacy 101: Practical Strategies for Improving Your Patient Materials

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#28: R&D QA Comprehensive Quality Strategy: An Approach to Managing Quality Risks Throughout the Drug Development Lifecycle

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