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Register to vote Register by 18 June to vote in the General Election on 4 July.
Explainer for businesses and persons regulated by the Veterinary Medicines Regulations 2013, as amended, on the transitional provisions included in the amending legislation: the Veterinary Medicines (Amendment etc.) Regulations 2024.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
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.
Report of the review of the evidence for dependence on, and withdrawal from, prescribed medicines.
Check if someone selling medicines online in Northern Ireland is allowed to do so by the Medicines and Healthcare products Regulatory Agency (MHRA)
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to register veterinary practice premises for veterinary surgeons to supply veterinary medicines.
A series of indicators to inform safer prescribing practice to help pharmacists, clinicians and patients review prescribed medication and prevent harm.
How to access the essential information you need when travelling to or living in Hong Kong as a British National.
This brief announces changes to UK VAT law allowing the zero rating for dispensing drugs prescribed by practitioners from the European Economic Area (EEA) and Switzerland.
If you've used illegal drugs or misused drugs you must tell DVLA - download the correct form to let them know
This series brings together all documents relating to drugs licensing.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
This Tax Information and Impact Note is about amendments to the scope of the zero-rate for drugs dispensed on the prescription of an appropriate practitioner.
Information about new applications, post-licensing, advertising, product information and fees.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
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