You can look for any word, phrase or Product Licence number (PL) using the search tool. You can also use the A-Z list to find the active substance. Every medicine pack includes a patient...

The new MHRA Safety Roundup provides a monthly summary of the latest safety advice for all medicines, medical devices, and healthcare products regulated by the MHRA, as part of our 3 …

The Review Panel: The Review Panel (MHRA) carries out statutory and non-statutory reviews of proposals, decisions and provisional decisions taken by Medicines and Healthcare Products …

2014年12月18日 · Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices. You may need to carry out a clinical investigation as part of …

This guidance document replaces the previous MHRA guidance titled “medical device standalone software, including apps”. As well as medical device apps becoming a growth area in …

Report a side effect with a medicine or medical device. Make a report. Loading results for ...

For breast cancer this includes cases diagnosed during current HRT use and diagnosed after HRT use until age 69 years; for other risks, this assumes no residual effects after stopping …

Organogram (organisation chart) showing all staff roles. Names and salaries are also listed for the Senior Civil Servants. MHRA organogram data is released by all central government …

Accompanying Guidance for MHRA Flow Chart of Clinical Investigations in Northern Ireland December 2024 Note [1] Pre-clinical or bench testing 1. Studies not involving humans are …

Each iDAP contains a complete listing of all suspected adverse reactions that have been reported to the MHRA via the Yellow Card scheme. This includes all reports received from healthcare...