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The MHRA products website allows you to find: The leaflets which are provided with medicines. The description of the medicinal product’s properties and how it can be used. Scientific reports...
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (21 May 2024) launched a four-week consultation which will support improved safety for certain high risk in...
We are the regulator of medicines, medical devices and blood components for transfusion in the UK. We put patients first in everything we do, right across the lifecycle of the products we...
The Medicines and Healthcare products Regulatory Agency (MHRA) is an executive agency of the Department of Health and Social Care in the United Kingdom which is responsible for ensuring that medicines and medical devices work and are acceptably safe.. The MHRA was formed in 2003 with the merger of the Medicines Control Agency (MCA) and the Medical Devices Agency (MDA). In April 2013, it merged with the National Institute for Biological Standards and Control (NIBSC) and was rebranded, with ...
Jan 28, 2015 · The Medicines and Healthcare Products Regulatory Agency (MHRA) website is now on GOV.UK.
PSUR. A Periodic Safety Update Report (PSUR) is a document which provides an evaluation of the risk-benefit balance of the medicine at defined times following authorisation. A searchable list of...
Welcome to MHRA-GMDP. The MHRA-GMDP database contains the following information issued by the MHRA relating to manufacturing and wholesale authorisations and certificates. Manufacturing and...
4 days ago · The MHRA’s (Medicines & Healthcare products Regulatory Agency’s) statement was published on 21 May 2024. Under the new proposal, the UK Government intends to allow certain medical devices that have been approved by international regulators to be placed on the GB market without obtaining a UKCA marking or UKCA certification.
Jan 9, 2024 · This new ‘roadmap’ for new regulations from the MHRA aims to enhance the UK’s ability to benefit from rapidly advancing medical technology, offering new opportunities for patients and healthcare. The MHRA’s roadmap sets out a route to deliver enabling regulation via a series of new Statutory Instruments (SIs).
Mar 21, 2023 · A series of new measures will be introduced by the Medicines and Healthcare products Regulatory Agency (MHRA) with support from partners to make it faster and easier to gain approval and...
