Content
In order to provide information on biocompatibility, many questions must be answered:
- What does the surface of the medical device look like?
- How do the production processes affect the surface?
- Which auxiliary and operating materials are used?
- Which ones become part of the surface and can no longer be removed?
- Which starting materials are toxicologically questionable (CMR substances), but the products are not?
- How do the process parameters have to be or be monitored?
Topic overview
- Basic, auxiliary and operating materials
- Reactions in the production process including process parameters and toxicity
- Estimation of the type and quantity of toxicologically questionable material components
- Process validation and monitoring (risk-based approach)
- Analytical options for characterizing the surface
- Cleaning processes that are specifically tailored to the expected contamination
- Laser marking and packaging
target group
All employees in medical technology in production, quality management and/or development.
Prior knowledge
Not required.
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
