The American Conference on Clinical Trials & Regulation of Medical Devices (CTRMD 2023) is dedicated to The Conference is of special interest to regulatory affairs, clinical trials, and quality assurance individuals working.
Key Topics
- Combining Regulatory/Clinical and Reimbursement Strategies
- Regulatory Updates and Trends
- Cybersecurity Trends and Updates
- Challenges in Regulating AI/ML Medical Devices
- Clinical Data vs. Real World Evidence
- First in Human/Pilot Study – Tips & Tricks
- Clinical Evaluation Process and Report
- Quality Management Systems and MDSAP
- Post-Market Activities – Do’s and Don’ts
- The Role of Risk Management in Pre- and Post-Marketing
- Usability/Human Factors Trends and Updates
Who should Attend
Attendees with responsibilities in:
- Clinical trials
- Regulatory affairs
- Quality assurance
