UK Posts Sovereign Regulatory System Proposals On Three Priority Areas
Patient safety and continuing access to products have steered UK Life Sciences Council advisory group proposals on recognition of overseas device approvals in Great Britain, speeding innovation to market and ensuring medtech regulatory system capacity.
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UK Proposal On Foreign Device Approval Recognition Due February
The Life Sciences Council has agreed to issue proposals on how the UK should recognize approvals granted by other trusted medical device regulatory jurisdictions. The need for speed in all matters relating to the UK’s sovereign medtech regulatory system has been stressed by the UK devices industry.
‘Project Glass Box’ - UK Reveals Roadmap For AI Medtech Regulation
The MHRA recently announced plans to review and reform how medical devices with AI or software components are to be regulated in the UK. Its new roadmap sheds light on how, exactly, it will deliver on these ambitions.
Podcast: German Hospital Reform Ushers In A Reimbursement ‘Revolution’
Germany is introducing a new system of paying for inpatient care, whereby funds will be allocated both to diagnosis related groups and to a provisional pot from which funds will be distributed according to the type of care delivered. In this podcast with Medtech Insight, Gabriel Flemming of Germany Trade & Invest explains what it all means for medtech.