This lecture describes the key changes regarding post market surveillance and what companies should do to meet their new obligations. After the course you can take a final test to receive your certification. Enjoy!
Post-Market Surveillance for Medical Devices in Europe
$49.00
- Course Type: Video Lessons
- Language: English
- Level: Advanced
- Session: year 2020
- Time: 0 - 1 Hour
Course Breakdown
| Section | Time |
|---|---|
| Introduction | 00:03:13 |
| PMS Requirements in the MDR | 00:02:25 |
| PMS vs PMCF | 00:05:33 |
| Economic Operators and PRRC | 00:06:22 |
| Post-Market Surveillance | 00:01:54 |
| PMS Plan: Content Requirements | 00:01:28 |
| Periodic Safety Update Report (PSUR) | 00:02:07 |
| Surveillance Audits | 00:01:26 |
| Timelines for the application of MDR provisions for PMS | 00:00:59 |
Exam and Certifications
- Final Test – Post-Market Surveillance for Medical Devices in Europe
- Certification
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