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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
$1724
Member price:
$1499
Related events
Fees
- #21: Leadership: How to Organize and Lead People in a Work Group $405
- #22: Successful Drug Development: Best Practices for Clinical Trial Design, Agency Interactions, and Regulatory Document Writing $405
- #23: How to Prepare for an FDA Inspection $405
- #30: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development $405
- #31: Preparing for a US FDA Advisory Committee Meeting $405
- #32: Influencing Culture, Avoiding Bureaucracy, and Encouraging Innovation $405
- #34: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports $405
- #35: Ethical Issues in Clinical Trials $405
- #40: Analysis of Safety Data from Clinical Trials $755
- #41: Quality Oversight of CROs-Clinical Vendors $755
- #42: Fundamentals of ANDA Submissions and FDA Expectations Under GDUFA $755
- #43: Clinical Statistics for Nonstatisticians $755
- #44: Risk Management and Safety Communication Strategies $755
- #45: The Good Pharmacovigilance Practices in the EU: Global Applications $755
- #25: Signal Detection: Identifying and Managing Safety Signals $405
Group Discounts
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Ways to register
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