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When entering the UK, you need to prove your medicine is prescribed to you if it contains a controlled drug - find out what proof you need to get.
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 .
Information on carrying medicine containing controlled drugs for individual travellers entering or leaving the UK.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Report a problem ('adverse incident') with a medical device or medicine to MHRA using the Yellow Card Scheme
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
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.
You must get permission to export certain drugs and medicines.
How the MHRA makes decisions on what is a medicinal product (borderline products).
Information about new applications, post-licensing, advertising, product information and fees.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Apply for an import certificate to import a medicinal product into the UK for veterinary use.
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 actions to take for sourcing medicines in different circumstances.
Apply for a promising innovative medicine (PIM) designation or scientific opinion for your medicine from MHRA.
Industry must notify the MHRA if they will not be using these flexibilities
Sets out medicines that cannot be exported from the UK or hoarded because they are needed for UK patients.
Don’t include personal or financial information like your National Insurance number or credit card details.
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