MHRA MedTech Regs blog: working together to advance safety, access and innovation
Posted by:
Joseph Burt, Posted on:
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Categories:
designated standards, Health Institution Exemption (HIE), IMDRF, IVD, Med Tech Regulations, Post-Market Surveillance, Pre-market statutory instrument
In our September MedTech regulations blog, MHRA Head of Diagnostics and General Medical Devices Joseph Burt seeks stakeholder feedback to two surveys and looks ahead to Autumn updates about the Pre-market statutory instrument, an IVD roadmap and the next IMDRF …