Clinical Investigators for PMCF studies

Uniting manufacturers, clinical sites & study investigators in the pursuit of medical device safety

  • Medical device manufacturers

    Find pre-approved clinical investigators to run your PMCF studies

    Find clinical sites

  • Clinical sites & investigators

    Get access to targeted medical device clinical research opportunities

    Join our network

Do you need help with your PMCF study?

Contact us

Benefits for medical device manufacturers

  • Extensive database of clinical investigators
  • Pre-approved for PMCF studies
  • Rapid on-boarding & study initiation
  • Access to broad range of clinical sites

Finding clinical sites willing to engage in PMCF studies can be challenging and time-consuming.

Our selected clinical sites are looking out for opportunities and are pre-approved for medical device PMCF studies. We can also match you directly with existing users of your product.

Find clinical sites

Benefits for clinical sites & investigators

  • Study experience for clinical professionals
  • Clinical prestige & compliant remuneration
  • Retain full control of approvals
  • Free to join & no obligation

Active participation in clinical research brings rewards for hospitals, clinicians and other healthcare professionals.

We help you find medical device manufacturers who are primed and ready to perform HRA-approved Post-Market Clinical Follow-up PMCF studies at your hospital.

Join our network


We have compiled some of our frequently asked questions. If you'd like to know anything else about what we do, feel free to ask us a question.

  1. No. Clinical sites and investigators are free to join our network and retain full control over which studies, if any, are initiated at their site. Manufacturers are free to consider our recommended sites and pay only when they and the clinical site agree to move forward on the study together.

  2. At the moment, yes. The introduction of new medical device legislation (the MDR) means that there is currently an acute need for manufacturers to conduct medical device Post-Market Clinical Follow-up (PMCF) studies. Our aim is to meet that need and ensure manufacturers can conduct the research they require while hospitals can gain from experience, prestige and industry partnerships through active research participation.

  3. You can - although, in many cases, this can be a slow, expensive and inefficient process. Not all clinical sites are aware of medical device PMCF and, compared to RCTs, participation can be seen as unattractive. Our database of approved clinical sites understand the need for medical device PMCF are are excited, motivated and ready to participate. All they need is the right manufacturer with the right study.

  4. Active participation in clinical research is great for professional development and enables clinicians and healthcare professionals to contribute directly to the promotion of medical device safety. Study participation will be compliantly remunerated and, because PMCF studies often run long-term, this can enable expansion of on-site research departments and provision of dedicated research staff.

Do you have any questions to ask our team?

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