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Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
What you need to do to supply authorised medicines from Great Britain to Northern Ireland.
Export controls on goods that can be used for torture or capital punishment.
Cipla (EU) Limited, UK and Pharmathen S.A. have informed the MHRA that the outer carton (box) of the product batches mentioned in this notification are missing the medicines legal classification for a Prescription Only Medicine (POM).
Antipsychotic drugs available in the UK, their side effects and their effect on dementia patients.
Report discarded syringes, needles and other drug related items in public places to your council
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
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.
The penalties if you are caught taking or dealing drugs - drug classification, fines and prison sentences
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
There are changes to the legislation of Reference Medicinal Products (RMPs) used to support abridged marketing authorisation applications
Industry must notify the MHRA if they will not be using these flexibilities
List of controlled goods that follow the normal import declaration rules if HMRC apply continuity plans due to system issues.
Sets out medicines that cannot be exported from the UK or hoarded because they are needed for UK patients.
Information about controlled drugs licences for companies that possess, manufacture, produce or supply controlled drugs in England, Wales or Scotland.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
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