Last week, Health Minister Baroness Gillian Merron has announced that draft regulations for the post market surveillance of medical devices will be laid before Parliament by the end of the year.
These draft regulations will place more stringent demands on manufacturers when reporting incidents to the MHRA. Higher risk devices will also be subjected to additional surveillance.
More updates will be released later in the year and we will ensure BIVDA members are kept abreast of any developments.
