2021 - 6-Hour Virtual Seminar on The New EU Medical Device Regulation
Date2021-01-06
Deadline2021-01-04
VenueFremont, USA - United States
KeywordsMedical Device; Clinical Trial Managers; Virtual Seminar
Topics/Call fo Papers
The revisions therefore affected all kinds of medical devices including in vitro diagnostic medical devices, from home-use items like sticking plasters, pregnancy tests and contact lenses, to X-ray machines, pacemakers, breast implants, hip replacements and HIV blood tests.
This Seminar will look at what to expect when the new regulation is implemented. Including: 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.
This Seminar will look at what to expect when the new regulation is implemented. Including: 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.
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Last modified: 2020-12-15 18:39:14