Scientific Advice Meetings: A Guide to Successful Interactions with FDA, EMA and Beyond
One meeting. One shot. No second chances.
In drug development, your greatest challenge may be the meeting, not the molecule. Whether with FDA, EMA, or others, regulatory advice meetings are high-stakes, high-impact, and unforgiving. The outcome can fast-track your project or bury it in costly delays.
This guide helps you win that meeting.
Scientific Advice Meetings is the definitive playbook for biotech, pharma, and regulatory professionals navigating global regulatory interactions. Inside, you'll find:
- A detailed, step-by-step framework: From idea generation to post-meeting debriefs, we cover every critical stage.
- Strategy design tools: Learn to crystallize your regulatory objectives, align your team, and craft persuasive positions that regulators will respect.
- Expert writing guidance: Master the art of the briefing book: logic chains, persuasive framing, and regulator-ready narratives.
- Value for all levels: Whether you're leading your first interaction or refining your approach as a veteran, this book offers both foundational knowledge and seasoned insights.
What's inside:
- Chapters 1-2: Core concepts and regulatory landscapes for the major players (FDA, EMA, PMDA, NMPA) and the critical expectations that shape outcomes.
- Chapter 3: Crafting a winning strategy and securing internal alignment.
- Chapters 4-5: Building your application and briefing book for maximum persuasive impact.
- Chapters 6-7: Preparation for the meeting - rehearsals, challenge sessions, and adapting to preliminary feedback.
- Chapters 8-9: Best practices for the meeting itself and post-meeting actions.
- Appendices: Writing skills, review best-practices, and advanced problem-solving skills.
Don't guess. Don't improvise. Prepare.
The success of your drug program could depend on one conversation. Let this book help you make it count.
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