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Register to vote Register by 18 June to vote in the General Election on 4 July.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
Guidance for healthcare professionals on managing specific medicines and medical devices and using them safely.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
How we will manage exports if there's a shortage of supply.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Placing a veterinary medicine on the market, including non-medicinal products, medicinal words and phrases, how to obtain advice, report non-compliance.
Guidance on applications and licences for manufacturers & wholesalers, suspended and revoked licences, registrations, exporting medicines, defective medicinal products and fees.
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
New evidence on the pattern of local and imported supplies to different health sectors and via different supply chains in Tanzania
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
The Medicines and Healthcare products Regulatory Agency regulates medicines, medical devices and blood components for transfusion in the UK. MHRA is an executive agency, sponsored by the Department of Health and Social Care .
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
Guidance for industry on flexible approaches we are taking on good distribution practices.
Guidance for owners and masters about potentially hazardous medical supplies.
Check the legal requirements you need to meet before you can place a medical device on the market and see how MHRA monitors compliance.
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