‘Medtech For Unmet Needs’ Prioritized In New UK Industry Initiative
SMEs in the UK now have another source of business planning and innovation support.
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The MHRA has published more guidance on UKRPs and UK product registrations to help medtech companies navigate the new system and continue to reach the market.
How UK and EU device regulations will differ in 2021, UK approved bodies and Northern Ireland's unfettered access to the UK market were key themes at the ABHI’s annual regulatory conference.
The Swedish liquid biopsy start-up expects to be the first company to secure US FDA approval for a metabolism-based urine test for the early detection of kidney cancer in post-surgery patients.