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Registration fees
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Non-Member Price
$1989
Member price:
$1759
Related events
Fees
- #20: Leadership: How to Organize and Lead People in a Work Group $415
- #21: Successful Drug Development: Best Practices for Drug Development Planning, Agency Interactions, and Regulatory Document Writing $415
- #22: How to Prepare for an FDA Inspection $415
- #23: Signal Detection: Identifying and Managing Safety Signals $415
- #24: The Evolving Role of Payers in Drug Development: Pricing, Pharmacoeconomics, and Health Technology Assessment $415
- #30: Preparing for a US FDA Advisory Committee Meeting $415
- #31: Influencing Culture, Avoiding Bureaucracy, and Encouraging Innovation $415
- #32: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports $415
- #40: Clinical Statistics for Nonstatisticians $770
- #25: Regulatory Considerations for Drug Development: Current Status and Trend of IND/NDA Practice in China $415
- #33: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development $415
- #34: Implementing a Risk-Based Monitoring Solution: Understanding the Basics of a Sustainable Model $415
- #42: Analysis of Safety Data from Clinical Trials $770
- #43: The Good Pharmacovigilance Practices in the EU: Global Applications $770
- #26: Smart, Innovative Risk-based Auditing: Shifting the Paradigm $415
- #35: Digital Health Technologies for Combination Products and Beyond: Development and Regulation $415
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