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Emerging Trends in Global Regulations: Insights Into More Efficient Regulatory Writing Practices
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Understanding FDA: Essentials for Briefing Books in Pre-IND, Pre-NDA, and Pre-BLA Meetings
42:23
Real-World Data and Real-World Evidence 101
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Considerations for Companion Diagnostics: Lessons Learned and Key Takeaways from DIA 2024
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Good Science vs. Bad Writing: Strategies for Building an Effective Scientific Writing Team
58:06
MVC Post Discharge Follow Up Workgroup 12/3/24
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Post-market surveillance as a medical device requirement in the EU
36:11