Question to the Department of Health and Social Care:

To ask the Secretary of State for Health and Social Care, with reference to the report of the Independent Medicines and Medical Devices Safety Review report entitled First Do No Harm, published in July 2020, what recent steps he has taken to progress implementation of recommendation seven of that report on establishing a central patient-identifiable database.

NHS Digital has put together a programme of work to establish an information system to collect information on surgical implants and devices from healthcare providers in England, currently focussed on pelvic floor, or mesh and related procedures, as a priority.

This will be followed by the development of a United Kingdom-wide Medical Device Information System (MDIS) with regulations being made under section 19 of the Medicines and Medical Devices Act 2021. This system will mean that in future, subject to regulations, we can routinely collect medical device, procedure and outcome data from public and private provider organisations across the UK and data submitted directly from patients. Formal public consultation on the MDIS regulations will begin later this year with the aim of laying the regulations in due course.