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Register to vote Register by 18 June to vote in the General Election on 4 July.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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.
Prescribing or supplying veterinary medicines including requirements for registration and inspection of premises.
Information about new applications, post-licensing, advertising, product information and fees.
Information for wholesale dealer licence holders about the medicines put on the UK market for UK patients that they cannot export or hoard.
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
The VMR sets out the statutory fees associated with various regulatory services provided by the VMD. The statutory fees and fee structure are implemented from 17 May 2024.
Information on good laboratory, manufacturing and distribution practice, good pharmacovigilance practice (GPvP), out-of-specification investigations, inspection metrics and fees.
Details of certificates issued under the Special Import System for the top ten veterinary medicines that were imported 1 July - 30 September 2023.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
The legal text underpinning the regulation of manufacture, authorisation, marketing, distribution, use and post-authorisation surveillance of veterinary medicines and medicated feed.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Actions that trial sponsors should consider to build resilience into clinical trial design
Information and guidance on a range of medical devices for users and patients.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
The actions to take for sourcing medicines in different circumstances.
Check what side effects people have reported when they've taken a medicine.
Don’t include personal or financial information like your National Insurance number or credit card details.
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