NEW REQUIREMENTS FOR SAFETY REPORTING DURING CLINICAL INVESTIGATIONS
This course highlights new safety reporting obligations introduced by the Medical Device Regulation.
Surmodics Investigator Training for Adverse Event Reporting According to MDR
$999.00
- Course Type: Video Lessons
- Language: English
- Level: Advanced
- Session: 2022
- Time: 0 - 1 Hour
Course Breakdown
| Section | Time |
|---|---|
| Introduction | 00:05:43 |
| MDR Overview, Definitions, and Assessments | 00:10:58 |
| How to Collaborate with Sponsor | 00:05:00 |
| Schematic of the Reporting Process Final Summary | 00:02:32 |
| New SAE Reporting Requirements for Device Trials in Germany | 00:05:26 |
Exam and Certifications
- Take the Quiz!
- Course Certification
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