Build your MDR compliance package
Through our bespoke Post-Market Surveillance (PMS) service we will apply clinical knowledge to design, update, implement, and maintain your MDR compliant PMS systems.
Post-Market Clinical Follow-up
Our medical experts will design a robust and adaptable clinical evidence generation system to collect Post-Market Clinical Follow-up (PMCF) data on your medical devices.
Our full Clinical Evaluation service involves a 360-degree analysis of your medical devices, writing and reviewing CERs, and designing clinical development plans.
Our medics will apply powerful clinical techniques to quickly and effectively identify and minimise any gaps in your clinical evidence portfolio.
Use our MDR Requirements Matcher to see which General SPRs apply to your products
Why we are different
We are expertly-trained medical doctors who recognise the crucial role played by medical devices in the provision of quality healthcare. Read more about us
Our founder, Dr Paul Hercock, has applied his extensive training in medicine, law and medical devices to build a comprehensive platform of expert MDR compliance support services.
This expertise is leveraged through our network of specially-trained medical doctors who work within this platform to apply their clinical acumen to your products.
We match you to an expert clinician who is always available to you to produce the MDR compliance strategy that incorporates medical insight where it is needed most.