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The Marine Management Organisation (MMO) is conducting a programme to assess vessel monitoring systems to identify devices that meet its technical specifications for reporting of location, heading and speed by under 12m fishing vessels.
We’re working to help people securely prove who they are without having to rely on physical documents.
An overview of the future requirements for rapid COVID-19 diagnostic assays for antigen lateral flow devices.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
The Medicines and Healthcare products Regulatory Agency (MHRA) has today (9 May 2024) launched AI Airlock, its new regulatory sandbox for AI as a Medical Device (AIaMD).
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Guiding principles for the use of Predetermined Change Control Plans (PCCPs) for managing rapid product changes.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Information to support commercial fishers on under 12 metre English vessels.
Advice on writing clear notices and maximising replies to your FSNs.
Government outlines action to make UK a world leader in tackling ethnic and other biases in medical devices.
Support for SMEs in, or looking to enter, the medical technologies market.
Guidance on defining intended purpose for Software as a Medical Device (SaMD), to help SaMD manufacturers in meeting their statutory obligations.
Information to help schools, colleges, local authorities and trusts manage routers they received from DfE.
How to use a patient-reported outcomes and experiences study to evaluate your digital health product.
This page includes summaries of the winning bids for the Future RAN (FRANC) competition
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