Our Services within the Medical Technology


We supports you in your efforts to comply regulatory requirements of the EU, Canada and the US; and to bring your medical device on the market.

Including CE and UKCA marking of medical devices  

  • (EU) 2017/745 - MDR (CE Marking medical device)
  • (EU) 2017/746 - IVDR (CE Marking in vitro diagnostic device)
  • MDR/IVDR + Article 15 (PRRC – ‘Person Responsible for Regulatory Compliance’)
  • 'Responsible Person' as required by the MHRA (after the Brexit) 
  • 510(k)
  • Clinical evaluation 
  • PMS / Vigilance processes / PMCF
  • EU Authorized Representative services
  • FSC (Free Sales Certificate)
  • Quality Management System (ISO 13485)

Please contact us for more information.

FullServiceModel MRM


The deadline for compliance completion in accordance with the new EU Medical Device Regulation (EU) 2017/745 by medical device manufacturers is 26 May 2021.

This means that your company has limited time to:

1)      Implement an ISO 13485 Quality Management System

2)      Update product technical documentation file, which will need to include far more technical information than ever before.

The New EU Medical Device Regulation (EU) 2017/745 is NOT a new regulation that covers the old medical device directive 93/42/EEC (MDD) with a few changes and updates.  This new document is the result of four years of re-writing of medical regulatory requirements by the EU Authorities and includes registration and documentation upload in the EU Databank, including pre-clinical and clinical data, post-market surveillance plan and documentation, major changes to labeling including UDI codes, etc. etc.

Taking into account that it takes the average small manufacturer about ten to twelve months to implement an ISO 13485 quality management system and at least six months minimum to prepare a new technical documentation file, the time has come to start the process immediately.

If you have any questions or need any assistance, please let us know.

We stand ready to submit our proposal if you are interested.


  • UKRP-services
      The UK medical device regulatory system is independent of the European Economic Area (EEA). All medical device manufacturers will need to follow UK laws for (in vitro) medical devices, based on the EU regulations EU-MDR 2017/745 and EU-IVDR 2017/746. All non-UK manufacturers must have a UK-based UK Responsible Person…