Watchdog official ‘said Gove wanted to circumvent process’ for Dyson ventilator - The former minister was giving evidence to ...

The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has put out a call for developers of artificial intelligence as a medical device (AIaMD) technology to join its new regulatory ...

Along with AI-Airlock, the MHRA is also working on two new guidance documents, called Good machine learning practice for medical device deployment and Best practice AIaMD development and ...

First Global Regulatory Approval of PrecivityAD2 for Use as an In-Vitro Diagnostic to Aid in the Diagnosis of Alzheimer’s Disease The PrecivityAD2 blood test is an analytically and clinically ...

The government has announced the appointment of Lawrence Tallon as the new Chief Executive Officer of the Medicines and ...

The UK Government has appointed Lawrence Tallon as Chief Executive Officer of the Medicines and Healthcare products Regulatory Agency (MHRA).

We will generally refer the question to the MHRA devices specialists, in order to do this we will need a copy of the study protocol. This can be an early draft of the protocol, so long as the ...

today announced the medical device registration from the United Kingdom’s Medicines and Healthcare products Regulatory Agency (UK MHRA) for the PrecivityAD2 ™ blood test.