Regulatory Requirements for Clinical Investigation and Post-Market Surveillance of Medical Devices
- Dates:
- Organizer:
- Saudi National Institute of Health (SNIH)
- Location:
- Online (Zoom Webinar)
- Specialty:
- Quality & Patient Safety
- Format:
- Online
Gain insights into key regulatory and clinical considerations in medical device development and post-market surveillance across the product lifecycle. Objectives: (1) Understand key regulatory and clinical considerations in medical device development; (2) Recognize the role of post-market surveillance within the medical device lifecycle after commercialisation; (3) Understand regulatory expectatio
