A health watchdog said Michael Gove wanted to “circumvent” the regulatory process to push through a bid by Sir James Dyson to ...

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 ...

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

During late 2024, the MHRA – as part of a broader consultation on routes to market – restated its intention for the future UK regulation of medical devices to rely on the work of four other ...

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

After six years at the helm of the Medicines and Healthcare products Regulatory Agency (MHRA), Dame June Raine will step down ...

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

EXCLUSIVE: Scots vape firm VPZ warned a 'grey area' in the incoming disposable vapes ban has seen alternative super-sized ...

Reading from an email sent by Graeme Tunbridge, director of devices at the MHRA in March 2020, counsel to the inquiry Richard Wald KC said: “CDL was keen to press forward with Dyson’s proposal ...

A health watchdog said Michael Gove wanted to “circumvent” the regulatory process to push through a bid by Sir James Dyson to supply NHS ventilators during the pandemic, the UK Covid-19 ...