Content
The regulations for placing medical devices on the market are continually evolving. The seminar provides an overview of the current status of the most important aspects when placing medical devices on the market. The event also offers the opportunity to discuss how to deal with the respective innovations in the group with an experienced speaker.
Topic overview
- Product life cycle – development process
- Technical documentation (Design History File, Device Master Record, Summary Technical Document)
- Classification of medical devices
- Conformity assessment procedures
- Post-market surveillance
- Clinical evaluation
- Biocompatibility
- Usability
target group
The seminar is aimed at quality management employees who are jointly responsible for placing medical devices on the market and want to update their knowledge of the requirements for this.
Prior knowledge
Previous knowledge about placing medical devices on the market is necessary.
Funding opportunity
ESF funding is possible. Further information can be viewed here .
Early bird discount
If you register up to 3 weeks before the start of the seminar, you will receive an early bird discount of 10 percent.
KONTAKT:
TuttlingenTuttlingen & Online
