At this BASG meeting, we will inform you about current and future developments in the field of clinical trials of medical devices and performance studies of in vitro diagnostics.
Contents
- Regulation (EU) 2017/745 for medical devices, specifically for clinical trials
- Regulation (EU) 2017/746 for in vitro diagnostics, specifically for performance studies
- Update on the EUDAMED module for clinical trials/performance studies
- National specifics, best practices and case studies
- Information from the European working groups (CIE)
- Exchange of experiences and discussion
The detailed programme can be found [url_begin|programme|link|here|url_end].
Target
- Employees of regulatory affairs departments at manufacturers of medical devices or in vitro diagnostics
- Employees of contract research organisations (CROs) and self-employed persons
- Employees of clinical trial coordination centres (KKS)
- Academic researchers
Language
German
Registration
Please register by [registration_start|registration|link|registration|registration_end] at the latest.
This event will be held exclusively online.
Technical management
Dr. Stefan Strasser
Clinical Trials Department, Institute for Monitoring
Medical Market Surveillance
AGES GmbH