Webinars

Search results on Pharmaceutical Regulation

423 Results

October 15, 2024

Changes to the FDA guidance on Data Monitoring Committees in clinical trials
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October 07, 2024

Modular CMC Development for Antibodies: Deploying a Purpose-Designed Path to Clinic
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October 07, 2024

Diversity Action Plan Success: From Planning to Execution
October 07, 2024

Multi-sponsor Pregnancy Exposure Registries: Physician, Scientific Advisory and Industry Insights
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October 03, 2024

Pharmacovigilance in a Global Market: Key Compliance Strategies
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September 27, 2024

Global R&D Insights in Drug Development: Insights from Industry on the Future of Pharma
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September 25, 2024

The New Era of Project Optimus: Implications for Oncology Development Strategy
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September 24, 2024

Managing Compliance Risk in Life Sciences: How Can IT and Quality Teams Root it Out
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September 24, 2024

The Journey to Approval: Navigating the Road from EoP2 to NDA Submission
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September 20, 2024

Medicare Part D price negotiation update
September 19, 2024

Patient First: Enhancing Strategies for Effective Patient Engagement, Recruitment and Diversity in Clinical Trials
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September 17, 2024

Accelerating Clinical Product Development through Centralized Content Work Streams
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September 12, 2024

Mastering RMPs and RMMs: Tech-driven solutions for patient safety
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September 11, 2024

Clinical Data Analysis: Avoiding Obstacles to Success
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September 11, 2024

Beyond Numbers: The Value of In-Trial Interview Data for Regulatory and Health Technology Assessment (HTA) Decision-Making
September 10, 2024

Regulatory Submission Writing for NDA Success
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September 09, 2024

Strategic Advantages of Early-Phase Oncology Clinical Development Across Australia and the USA
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September 09, 2024

Why Authenticity and Patient Voice Are Critical When Driving Clinical Trial Diversity
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September 05, 2024

Advancing Precision Oncology: Radionuclide Conjugate and Antibody-Drug Conjugate (ADC) Development Strategies
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September 04, 2024

Considerations for Oligonucleotide Therapeutics in CMC