Post market surveillance (PMS)

Post market surveillance is an increasingly important area of the medical device lifecycle and much more emphasized in EU MDR 2017/745.

We can help you with:

  • Draft or review PMS procedures and plans
  • PMS report reviews
  • Training

Contact me for further information
Nils-Åke Lindberg
Office +46 8 621 01 05 or send me an e-mail