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Register to vote Register by 18 June to vote in the General Election on 4 July.
Reported problems with the supply of an animal medicine and the date when the issue is expected to be resolved.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How an innovative funding mechanism is saving lives by speeding up the availability of vaccines and making them affordable.
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...
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
For manufacturers and distributors of intermediate and final feedingstuffs containing a medicinal premix or specified feed additives.
How we evaluated pre-exposure prophylactic (preventative) treatments for COVID-19.
VDEC developed a standardised assay reduce the development of antimicrobial resistance and improve patient treatment for tuberculosis.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
Information about new applications, post-licensing, advertising, product information and fees.
Check the tariff classification for preparations put up for retail sale.
How to spot contagious equine metritis, what to do if you suspect it and measures to prevent its spread.
How to comply with the exemption from the Veterinary Medicines Regulations that allow certain animal medicines to be sold without a marketing authorisation.
Urgent safety updates arising from pharmacovigilance data, including reported adverse events, for veterinary medicines authorised in the UK.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines in the UK.
Details of the process changes for established medicines, effective from 1 March 2024, which apply specifically to chemical products.
Guidance for prescribing vets on the use of the cascade.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Lists published of the ten products for which most Special Import Certificates (SIC) have been issued each quarter in previous year.
The Commission on Human Medicines (CHM) advises ministers on the safety, efficacy and quality of medicinal products. CHM is an advisory non-departmental public body, sponsored by the Department of Health and Social Care .
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