UK Responsible Person (UKRP)

As a UK Responsible Person we will commit to the following (as in line with UK MDR 2002):

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• ensure that the Client has put in place an appropriate declaration of conformity along with the correct technical documentation for their product and, where applicable, that an appropriate conformity assessment procedure has been applied;

• register the Client’s devices with the MHRA;

• keep available a copy of the Client’s technical documentation, a copy of the declaration of conformity and, if applicable, a copy of relevant certification, including any amendments and supplements for inspection by the MHRA;

• in response to a request from the MHRA, provide the MHRA with all the information and documentation necessary to demonstrate the conformity of a Client’s device;

• respond to requests from the MHRA and forward any MHRA requests for samples or access to a device to the Client, ensuring that the MHRA requests are fulfilled;

• cooperate with the MHRA on any preventive or corrective action (CAPA) taken to eliminate or, if that is not possible, mitigate the risks posed by Client’s devices;

• immediately inform the Client about complaints and reports from healthcare professionals, patients and users about suspected incidents related to one of their devices.