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How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
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.
As a vet or pharmacist, you must follow legal requirements when working with controlled drugs in veterinary medicine.
Legal requirements and good practice guidance for SQP retailers’ premises inspections.
Besins Healthcare (UK) Ltd has informed the MHRA that a defective pump system was detected in two batches of Oestrogel Pump-Pack 750 micrograms/actuation Gel.
How to prepare for implementation and compliance of the Safety Features Regulation.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
The Advisory Council on the Misuse of Drugs makes recommendations to government on the control of dangerous or otherwise harmful drugs, including classification and scheduling under the Misuse of Drugs Act 1971 and its regulations. ACMD is an advisory non-departmental...
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Doncaster Pharma Limited have identified an error relating to the Braille printed on the cartons on various parallel imported packs which have been repackaged by BModesto B.V.
How a marketing authorisation holder should report a defect with a veterinary medicine.
Information for patients, healthcare professionals and developers of new medicines
Urgent safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Guidance for prescribing vets on the use of the cascade.
Prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
Details of the Yellow Card scheme, which is the system for recording adverse incidents with medicines and medical devices in the UK.
How the MHRA makes decisions on what is a medicinal product (borderline products).
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