Ask the Expert: The Role of Real-World Evidence (RWE) in Regulatory Submissions
50:20
Devices in Focus: How to Save Time & Money with Real World Evidence
59:31
Understanding FDA: Essentials for Briefing Books in Pre-IND, Pre-NDA, and Pre-BLA Meetings
51:16
Overcoming Deadline Bottlenecks in Pharma: How a Writing Team Can Help
53:57
IVDR in Focus: Tips for Performance Evaluation Planning to Support Your Transition from IVDD to IVDR
42:23
Real-World Data and Real-World Evidence 101
48:17
Practical Strategies to Successfully Navigate Key IVDR Regulations Applicable to SaMD Devices
52:08
Considerations for Companion Diagnostics: Lessons Learned and Key Takeaways from DIA 2024
45:45