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Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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.
Pharmacy, prescription-only (POM), and general sale list (GSL) medicines: apply to move your medicine to a different classification.
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.
Guidance for prescribing vets on the use of the cascade.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
Explains changes to drug driving law and the guidance available for healthcare professionals and users of prescription medicine.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without an authorisation.
How marketing authorisation holders should inform MHRA of a signal or an ADR to a medicine.
Guidance on prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
Advice for medical professionals to follow when assessing drivers with psychiatric disorders.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
This guidance provides information on comparator products used in studies supporting abridged marketing authorisation applications
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