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Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Sign up for alerts about applications for UK trade marks or international registrations
Apply for a grant-aided vessel monitoring system, register or re-register your device, and guidance for manufacturers and engineers.
What to do if you have an electronic tag (including curfew tags, location tags and alcohol tags) and how to contact the Electronic Monitoring Service (EMS).
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to use an interrupted time series to evaluate your digital health product.
New satellite-enabled ankle tags are being rolled out in phases across England and Wales by the Ministry of Justice.
Information and guidance on a range of medical devices for users and patients.
Manufacturers should use these forms when a device is released to a vessel owner and to confirm a device has been installed and is working.
Information on road traffic devices, such as breath-testing, speed cameras and immobilisation devices.
Information about the EU Regulations and their implementation in Northern Ireland
Advice for manufacturers of Class I medical devices for placing products on the UK market
Check the tariff classification of multifunctional display-monitors for vehicles.
What you need to do if you manufacture or import tobacco products in the UK.
Guidance on choosing evaluation study types and methods.
A research paper from the CMA
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
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