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Medicines and Healthcare products Regulatory Agency

Laura Squire

April MedTech regulatory reform update: international recognition, IVDs and AI

Posted by: , Posted on: - Categories: Conferences and events, Improving Our Services, Med Tech Regulations, Medical Devices

Last time I wrote was just before we headed to Washington DC for the 25th Session of the International Medical Device Regulators Forum (IMDRF), hosted by the US Food and Drug Administration (FDA). The first two days were a workshop …

Med Tech Regulatory Reform: Webinars, Trusted Advisors and Heading to Washington

Posted by: , Posted on: - Categories: Innovation, Med Tech Regulations

  Welcome to the March issue of the Med Tech Regulatory Reform blog series. As the leader of a team which includes many talented female scientists, I am particularly delighted to be publishing this at the start of British Science …

Med Tech Regulatory Reform: The first steps towards a new framework for medical devices in the UK

Posted by: , Posted on: - Categories: Med Tech Regulations, Medical Devices

On 9 January 2024, the Medicines and Healthcare products Regulatory Agency (MHRA) published its Roadmap for the delivery of the future regulatory framework for medical devices. In the first of a new blog series, Laura Squire, Med Tech Regulatory Reform …

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