medical.device.forum
The medical.device.forum is designed for professionals responsible for quality management, regulatory affairs, risk management, and product management and provides support for the implementation of current regulatory requirements for medical devices.
The forum addresses not only the legally compliant implementation of the MDR but also the regulatory aspects of digitalization in medical devices. Get comprehensive information from representatives of authorities, TÜV SÜD-experts, medical device manufacturers and lawyers.
You can find the detailled agenda on the German website.
Please note: the conference language is German only.
- current status of the implementation of MDR
- combined products: critical questions at the medical device / pharmaceutical interface
- Challenge with ISO 13485, 14971, 10993
- Biocompatibility assessments according to MDR and ISO 10993
- regulatory frame for medical device software with artificial (AI)
- Cyber security / IEC 81001-5-1 & IEC TR 60601-4-5
- Data security and data protection requirements for DiGA
- Manufacturers of medical devices
- Distributors and operators of medical devices
- Representatives of authorities
- Clinical research organizations in the medical device sector
TÜV SÜD
Algorithmus Building
Rüdesheimer Str. 10
80686 Munich, Germany
At our exhibition, which runs alongside the event, you can showcase your company, products and services. Stands measuring 5 m² are available to book. Further information can be found on the German website.