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
Steps to help grow your business - finding finance, mentors, increasing sales and developing products and services
When HMRC will issue a joint and several liability notice to individuals who have been involved with companies which have become insolvent and have a tax liability with HMRC.
The MHRA will review applications for orphan designation at the time of a marketing authorisation (MA) or variation application.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How to market eggs, including rules on registration, egg marking, salmonella control and egg marketing inspections in England and Wales.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Guidance on applying to renew a marketing authorisation (MA) for a veterinary medicine.
Use the rolling review route when you want to submit your eCTD dossier in separate parts for pre-assessment instead of making a full consolidated document submission.
Guidance for suppliers and dealers.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to market forest reproductive material (FRM) for forestry purposes, including regulations, registration, master certificates and licences.
The CMA has today published its main concerns following an initial review into the veterinary sector.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
Submissions related to human medicines need to be submitted directly to the MHRA.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
From 13 May 2024 we are introducing a change to the procedure for new Marketing Authorisation (MA) applications, where a joint assessment of labels is requested.
How to use a multiphase optimisation strategy (MOST) to evaluate your digital health product.
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.