Requirements of the legislation 1.
Medical device clinical trials uk.
Clinical investigations of medical devices january 2020 3 18 clinical investigation in the uk.
Clinical trials of medicines and medical devices clinical studies that look at investigating the effects of drugs or medical devices are subject to uk and eu law.
They are regulated in the uk by the medicines and healthcare products regulatory agency mhra and require nhs ethics approval before the study can start through the health research.
The main types of clinical investigations for medical devices are outlined below.
Health research ranges from simple questionnaires and screenings to clinical trials of investigational drugs and devices.
Under the current medical device.
Clinical trials and investigations detailed information gov uk skip to.
Learn more about european medical device regulations at emergo group.
Explore current studies at uk and request information on opportunities that interest you.
This includes devices used in clinical trials of medicines to stratify patients for inclusion exclusion in the trial or stratified to a cohort within a trial.
Clinical trials for medical devices.
List of information about clinical trials and investigations.
In order to be able to ce mark any device a manufacturer must demonstrate that the stated device complies with the relevant essential requirements of the european directives.
Join us in discovery.
What are the types of clinical trials involving medical devices.
The health research authority hra in the uk is now requiring registration of clinical trials for some medical devices.
Office of device evaluation.
Search open clinical trials at uk using trialstoday.
The table below provides a side by side comparison of pharmaceutical trial phases versus medical device trial stages.
Hungarotrial is a full service cro for medical devices including clinical trials regulatory service and market access service for eu market.
Division of cardiovascular devices.
This is a limited clinical investigation of a device early in development typically before the device design has been finalised for a specific use.
Medicines medical devices and blood regulation and safety.