The International Conference on Clinical Trials and Regulations of Medical Devices and IVD (CSMD) covers topics such as:
- Combining Regulatory and Reimbursement Strategies
- Regulatory Updates and Trends
- Challenges in Regulating Digital Health Products
- Technical Documentation and Pre-Market Applications
- Quality Management Systems and MDSAP
- Clinical Data vs. Real World Evidence
- The Role of Risk Management in Pre- and Post-Marketing
- Clinical Evaluation Process and Report
- Vigilance and Post-Market Surveillance
The International Conference on Clinical Trials and Regulations of Medical Devices and IVD (CSMD) brings together senior attendees from regulatory bodies, academia, and industry.