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PMS plans and reports

The PMS of your medical devices must be carefully planned and documented. This is required not only by the MDR but by several MDCG guidelines and ISO/TR 20416 as well. The PMS and the separate PMCF plan describe how data should be collected and evaluated. Notified bodies check both documents during the quality management system audit. 

Putting the pieces together

Our services include the evaluation of your PMS data, which are processed and statistically evaluated with our proven novineon CRO methodology.  We then create a trend report and summarize the results in a report. The MDR requires a PMS report for class I products and a regularly updated PSUR (Periodic Safety Update Report) for higher risk classes.  Due to the modularity of our approach, these reports can be directly integrated into the clinical evaluation.

 

Risk classType of reportFrequencyAddresseeEvaluation
IPMS reportas neededresponsible authority upon request
IIaPSURas needed, at least yearlynotified body + responsible authority upon request
IIbPSURyearlynotified body + responsible authority upon request
III/ImplantPSURyearlynotified body + EUDAMEDEvaluation by notified body; report + evaluation to responsible authority

Our services:

  • Pragmatic and compact summary of all necessary activities and methods in a PMS plan
  • Data preparation and evaluation
  • Creation and updating of PMS report or PSUR

Contact

Contact your novineon specialist.

Email: pms@ remove-this.novineon.com
Phone: +49 7071 98979 – 127