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Apply for an import certificate to import a medicinal product into the UK for veterinary use.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
The T28 exemption allows pharmacies and similar places to denature controlled drugs to comply with Misuse of Drugs Regulations 2001.
You must get permission to export certain drugs and medicines.
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.
Information and guidance on a range of medical devices for users and patients.
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
Guidance on prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
The Advisory Group on Military and Emergency Response Medicine (AGMERM) provides specialist advice to the Ministry of Defence on the medical aspects of defence against chemical, biological and radiological threats. AGMERM works with the Ministry of Defence .
The unit is a specialist in aerobiology, biocontainment and biosafety. The unit provides government departments and the commercial sector with expertise, advice and consultancy.
Guidance for UK wholesalers and manufacturers on how to import human medicines including unlicensed medicines, how to apply for a licence and how much it costs.
How investigators and sponsors should manage clinical trials during COVID-19
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
How to apply for approval for a suitably qualified person (SQP) retailer premises to sell or supply animal medicines.
How to account for VAT on goods and services provided by registered health professionals, including doctors, dentists, nurses and pharmacists.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
How to conform with the legal requirements for placing medical devices on the market.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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