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Non-Member Price
$2029
Member price:
$1799
Related events
Fees
- #40: Interdisciplinary Safety Evaluation During Product Development $785
- #42: Patient Preferences: Using Conjoint Analysis and Stated Preferences in Drug Development and Regulatory Decision Making $785
- #41: Toolkit Approach to Best Practices in Root Cause Analysis and CAPA Management Workshop $785
- #43: Back to the Future: Combination Products in the 21st Century $785
- #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? $425
- #21: Basics of European Medical Device Regulation $425
- #22: Protocol Co-Design with Patients and Advocates $425
- #23: Preparing for a US FDA Advisory Committee Meeting $425
- #24: Data Visualization in the Life Sciences $425
- #27: eCOA 101: The What, Why, and How of eCOA to Reduce Barriers to Adoption in Clinical Studies $425
- #30: Machine Learning in Pharmacovigilance $425
- #33: European Regulatory Meetings: How Best to Prepare and Perform $425
- #34: Implementing a Risk-Based Monitoring Solution: Understanding the Basics of a Sustainable Model $425
- #35: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Effecting Pharmaceutical Development $425
- #36: A Novel Interactive Safety Graphic to Evaluate Potential Drug-Induced Hepatotoxicity $425
- #37: Patient Literacy 101: Practical Strategies for Improving Your Patient Materials $425
- #28: R&D QA Comprehensive Quality Strategy: An Approach to Managing Quality Risks Throughout the Drug Development Lifecycle $425
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