Trending Topics: From the AI Act to Orphan Devices, Key Takeaways from RAPS EU Convergence 2024
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Ask the Expert: The Role of Real-World Evidence (RWE) in Regulatory Submissions
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EU AI Act Impact: Your Business Game Plan Now!
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Considerations for Companion Diagnostics: Lessons Learned and Key Takeaways from DIA 2024
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How to classify a Medical Device? (EU MDR Case Studies)
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Emerging Trends in Global Regulations: Insights Into More Efficient Regulatory Writing Practices
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Medical Device Regulations / FDA Approval
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AI Act : comment anticiper les prochaines étapes et la mise en conformité des technologies d'IA ?
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