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Non-Member Price

$1989

Member price:

$1759

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#20: Leadership: How to Organize and Lead People in a Work Group

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#21: Successful Drug Development: Best Practices for Drug Development Planning, Agency Interactions, and Regulatory Document Writing

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#22: How to Prepare for an FDA Inspection

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#24: The Evolving Role of Payers in Drug Development: Pricing, Pharmacoeconomics, and Health Technology Assessment

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#30: Preparing for a US FDA Advisory Committee Meeting

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#31: Influencing Culture, Avoiding Bureaucracy, and Encouraging Innovation

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#32: Preparation of Risk Evaluation and Mitigation Strategies Assessment Reports

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#40: Clinical Statistics for Nonstatisticians

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#25: Regulatory Considerations for Drug Development: Current Status and Trend of IND/NDA Practice in China

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#33: Japan Regulatory Environment: Overview of the Organization, Processes, Systems, and Changes Affecting Pharmaceutical Development

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#34: Implementing a Risk-Based Monitoring Solution: Understanding the Basics of a Sustainable Model

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#42: Analysis of Safety Data from Clinical Trials

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#43: The Good Pharmacovigilance Practices in the EU: Global Applications

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#26: Smart, Innovative Risk-based Auditing: Shifting the Paradigm

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#35: Digital Health Technologies for Combination Products and Beyond: Development and Regulation

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