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Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without a marketing authorisation.
You must get permission to export certain drugs and medicines.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
The way you apply to licence biological products has changed
Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
The eMIT provides information about prices and usage for generic drugs and pharmaceutical products.
Getting a work reference from an employer either while in work or when applying for a new job – and what you can do if you think it's unfair.
Information for companies on the import and export of controlled drugs to and from the UK.
Licence and registration application information for companies that deal in precursor chemicals.
The most commonly encountered drugs currently controlled under the misuse of drugs legislation.
This series brings together all documents relating to ACMD drug-specific reports.
Links to EU guidance, as it stood immediately before end of transition period.
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.
Taking warfarin and tramadol together can cause harmful drug interactions, which can raise the International Normalised Ratio (INR), and result in severe bruising and bleeding, which in some patients could be fatal.
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