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Register to vote Register by 18 June to vote in the General Election on 4 July.
How the supply of medical devices from Great Britain into Northern Ireland works.
Report on all regulations in force during the first reporting period made using the powers in specific sections of the act, including stakeholder feedback and the department’s response.
Links to EU guidance, as it stood immediately before end of transition period.
Anti-choking devices are intended to alleviate choking incidents after Basic Life Support protocols have been attempted and failed. There are numerous counterfeit and unbranded anti-choking devices being sold in the UK online which do not have a valid UKCA or...
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).
Checklists providing a practical guide to using medical devices.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
How a manufacturer can apply for approval to supply a non-compliant medical device on humanitarian grounds.
How to contact MHRA for specific services or enquiries.
This study compares the sourcing of local supplies and competing imports within the public, private and faith-based sectors
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Guidance on managing and using bed rails safely.
Information for manufacturers and users of medical devices containing plastic with DEHP phthalates.
What is considered off-label use of a medical device and examples of it.
Notices of publication and a consolidated list for designated standards for medical devices.
Guidance on the steps manufacturers and suppliers can take to ease supply shortages.
Guidance for industry and organisations to follow from 1 January 2021.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
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