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- #20: Japan's Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development $405
- #21: The Sunshine Act: Understanding the Essentials of Compliance $405
- #33: Bayesian Evidence Synthesis and Network Meta-analysis $405
- #23: Leadership: How to Organize and Lead People in Group Work $405
- #24: Successful Drug Development: Best Practices for Clinical Trial Design, Agency Interactions, and Regulatory Document Writing $405
- #22: Preparing for a US FDA Advisory Committee Meeting $405
- #30: Influencing Culture, Avoiding Bureaucracy, and Encouraging Innovation $405
- #31: Large-Scale Regulatory Functional Outsourcing: Emerging Trends, Challenges and Decision Criteria $405
- #32: Pharmacogenomics and Companion Diagnostics: The Future of Clinical Trials, New Product Development and the Practice of Medicine $405
- #35: Understanding Translational Medicine: Benefits and Innovative Approaches $405
- #34: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports $405
- #40: Analysis of Safety Data from Clinical Trials $755
- #41: Quality Oversight of CROs-Clinical Vendors $755
- #42: Regulatory Affairs for Biologics $755
- #43: Clinical Statistics for Nonstatisticians $755
- #44: Quality by Design: From Theory to Practice $755
- #45: Risk Management Plan $755
- #46: The Good Pharmacovigilance Practices In The EU: Lessons Learned and Frequently Asked Implementation Questions $755
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