From Brussels sprouts to mobility scooters: five tips from the MHRA for staying safe and well over the festive period

Ipca Laboratories UK Ltd has informed the MHRA that the Patient Information Leaflet (PIL) in the products listed in this notification do not contain all the required safety information.

An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.

Guidance for manufacturers of cardiac implantable electronic devices and their leads. It outlines specific scenarios that should be considered when determining if an incident is reportable.

Summary of the latest safety advice for medicines and medical device users

The MHRA is seeking evidence on the regulation of AI in healthcare to inform the recommendations of the National Commission into the Regulation of AI in Healthcare.

Guidance on the deadlines for initial and response submissions.