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PLANNING AN EFFECTIVE POST MARKET SURVEILLANCE PROGRAM FOR MEDICAL DEVICES

Location

Horsholm, Denmark

Date & Time

3 October 2017

Medicoindustrien is the Danish medical device industry association, and it holds regular training seminars for its members on device-related regulatory and associated matters. Following demand from its members, the Association held a one-day training event on the subject of post-market surveillance (PMS), covering subjects including:

  • The regulatory and business backgrounds
  • Defining a PMS strategy
  • Integrating PMS with the quality system
  • New requirements under the Medical Device Regulation

The speaker was Roger Gray, VP Quality and Regulatory, Donawa Lifescience Consulting. Pia Wissing Jensen, Chair of the Medicoindustrien PMS Group, also contributes a presentation on a practical approach to meeting the regulatory requirements.

Medicoindustrien is the Danish medical device industry association, and it holds regular training seminars for its members on device-related regulatory and associated matters. Following demand from its members, the Association held a one-day training event on the subject of post-market surveillance (PMS), covering subjects including: The regulatory and business backgrounds Defining a PMS strategy Integrating…