Surmodics Investigator Training for Adverse Event Reporting According to MDR

NEW REQUIREMENTS FOR SAFETY REPORTING DURING CLINICAL INVESTIGATIONS
This course highlights new safety reporting obligations introduced by the Medical Device Regulation.

  • 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

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  • Course Certification

Description

SURMODICS INVESTIGATOR TRAINING FOR ADVERSE EVENT REPORTING ACCORDING TO MDR

NEW REQUIREMENTS FOR SAFETY REPORTING DURING CLINICAL INVESTIGATIONS
This course highlights new safety reporting obligations introduced by the Medical Device Regulation.

Exclusive Training Course for Surmodics SWING Study

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