We use some essential cookies to make this website work.
We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services.
We also use cookies set by other sites to help us deliver content from their services.
You have accepted additional cookies. You can change your cookie settings at any time.
You have rejected additional cookies. You can change your cookie settings at any time.
Departments, agencies and public bodies
News stories, speeches, letters and notices
Detailed guidance, regulations and rules
Reports, analysis and official statistics
Consultations and strategy
Data, Freedom of Information releases and corporate reports
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
This note is part of the statutory guidance under s215 of the HRA 2008 (from 1 April 2024)
Check if you can apply for Authorised Use relief to reduce your payments when you import goods for a specific use. This can include repairs, maintenance or processing.
Check which Authorised Economic Operator status you could apply for and their benefits if your business has role in the international supply chain.
Immigration staff guidance on checking whether an asylum applicant's representative is legally authorised to provide advice.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Find out the different ways you can get client authorisation including the digital handshake, Online Agent Authorisation service, paper forms and through your client's business tax account.
What you need to do to supply authorised medicines from Great Britain to Northern Ireland.
Advice on writing clear notices and maximising replies to your FSNs.
This guidance covers ‘grandfathering’ and managing the lifecycle changes of medicinal products.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Find out about the different simplified declarations for imports and what you need to do to get authorisation to use them.
Find out how to use the Online Agent Authorisation to get client authorisation for HMRC online services for agents.
Responding to suspected breaches of planning control.
Apply for protection against infringements of intellectual property rights on imports into and exports out of the UK.
How legal industrial action is organised, picketing and the law and what your employment rights when you are on strike
Don’t include personal or financial information like your National Insurance number or credit card details.
To help us improve GOV.UK, we’d like to know more about your visit today. We’ll send you a link to a feedback form. It will take only 2 minutes to fill in. Don’t worry we won’t send you spam or share your email address with anyone.