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Registration fees
The prices below are industry pricing. Reduced pricing may be available for Nonprofit/Academia and Government, subject to eligibility verification. Click Register to get pricing appropriate for your work setting. Review the cancellation and transfer policy.
Non-Member Price
$1989
Member price:
$1759
Related events
Fees
- #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? $415
- #21: The IDMP Challenge: Points to Consider for Pharmacovigilance Departments $415
- #22: Protocol Co-Design with Patients and Advocates $415
- #23: R&D QA Comprehensive Quality Strategy: An Approach to Managing Quality Risks Throughout the Drug Development Lifecycle $415
- #24: Preparing for a US FDA Advisory Committee Meeting $415
- #25: Precedent: A Driver of Regulatory Strategy $415
- #27: The Evolving Role of Payers in Drug Development: Pricing, Pharmacoeconomics, and Health Technology Assessment $415
- #28: Preparing Documents for Disclosure and Public Sharing $415
- #29: Leadership: How to Organize and Lead People in a Work Group $415
- #30: Implementing a Risk-Based Monitoring Solution: Understanding the Basics of a Sustainable Model $415
- #31: Machine Learning in Pharmacovigilance $415
- #33: Quality Tolerance Limits/Issue Management: Taming the Beast of Clinical Development Risk $415
- #34: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Effecting Pharmaceutical Development $415
- #36: Value Pricing Bootcamp: A Crash Course in How to Use Real World Evidence to Better Measure Outcomes and Evaluate New Innovative Therapies $415
- #37: Data Visualization in the Life Sciences $415
- #35: FDA Advisory Committee Purpose and Noninferiority Case Study: Rivaroxaban $415
- #40: Smart, Innovative Risk-Based Auditing: Shifting the Paradigm $770
- #42: Back to the Future: Combination Products in the 21st Century $770
- DIA 2018 Community Service Opportunity $0
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