Officers from the Hunan Provincial Food & Drug Administration paid a visit at Michor Consulting in Vienna in order to discuss
the regulation of medical devices on R&D, the registration regulation in Austria/EU,
the incentive system and the management system for devices manufacturers
and the importation of medical devices from the EU into the Chinese health care market.
This Seminar will look at what to expect when the new EU regulation is implemented: The transition period, Effect on Notified Bodies, Impact of the MDR on Quality Management Systems (QMS), technical documentation, clinical trial requirements, UDI and combination products.
Details & booking