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Get help to classify herbal medicines, vitamins, food preparations, supplements and tonics for import and export.
The MHRA has authorised cabotegravir as 30 mg tablets and as a 600 mg long-acting injection administered every two months
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Wet line contamination involves the cross contamination of road fuel with rebated fuels, which will either be red diesel or kerosene.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
Check the tariff classification for peptide nisin standardised with sodium chloride
Winners of DWP’s Disability Confident Awards crowned in night of disability employment celebration.
UK government interpretation of the requirements for labelling e-liquids for Northern Ireland.
Marketing standards for poultry meat producers, manufacturers, retailers and distributors.
How bottled water producers can get a natural mineral water recognised in England, and rules you need to follow to produce and label it.
Healthcare professionals should be vigilant for suspected adverse reactions and safety concerns associated with e-cigarettes and e-liquids, commonly known as vapes. Please report adverse reactions to the Yellow Card scheme and promote vigilance among patients.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 Oct - 31 Dec 2023.
News and guidance on veterinary medicines issues affected by coronavirus (COVID-19).
How to apply for marketing authorisation via this new procedure.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Pharmacovigilance system requirements
Information on cleaning an oil spill including your options, how to get a product approved and how long it will take.
Search for information about medicines including patient information leaflets (PILs), details on how the medicine can be used (SmPCs) and scientific reports (PARs).
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
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