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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
$1525
Member price:
$1350
Related events
Fees
- #20: Japan's Regulatory Environment: Overview of the Organization, Processes, Systems and Changes Affecting Pharmaceutical Development $405
- #21: FDA Enforcement: Understanding the Agency's Authority, How Violations Occur, How to Prevent Them and How to Respond if Violations Do Occur $405
- #22: Global Reimbursement Systems: A Market Access Perspective $405
- #23: A Device Primer: 510(k)s, PMAs, IDEs $405
- #25: Leadership: How to Organize and Lead People in Group Work $405
- #30: Analysis of Safety Data from Clinical Trials $405
- #31: Highlights of the New Pharmacovigilance Legislation in the EU: Key Points to be Taken into Account for Successful Implementation and Lessons Learned $405
- #32: Understanding Translational Medicine: Benefits and Innovative Approaches $405
- #34: Fourteen Steps from Research to Development $405
- #50: Understanding and Navigating the Regulatory System in China $755
- #51: Quality Oversight of CROs-Clinical Vendors $755
- #52: Regulatory Affairs for Biologics $755
- #53: Clinical Statistics for Nonstatisticians $755
- #54: Art of Writing a Clinical Overview $755
- #55: Overview of Drug Development $755
- #56: Risk Communications $755
- #57: Preparing for a US FDA Advisory Committee Meeting $755
- #40: Investigative Site Boot Camp: Innovative Solutions to your Operational Challenges $350
- #41: The DIA - HBA Skill Building Series: A Custom-Fit Leadership Approach for Women in the Regulatory, Medical, Legal and Compliance Functions $350
- #35: Successful Drug Development: Best Practices for Clinical Trial Design, Agency Interactions and Regulatory Document Writing $405
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