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
Register to vote Register by 18 June to vote in the General Election on 4 July.
The effectiveness of marketing channel liberalization in increasing competition among traders and prices obtained by farmers for their produce
Find out if your business needs to publish a tax strategy, what it should include and when to publish it.
A systematic review and contextualisation of review findings to South Asia and Nepal
This section provides guidance for communications network providers on legislation, regulation, working with local authorities and with property developers.
How the MHRA assesses Marketing Authorisation Applications (MAA) for medicines referred under Article 29.
This playbook explains how we use social media at GDS. In it, we share our best practice, what we've learned and what we're planning to do.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
This strategy sets out our vision of the role of the retail market in achieving net zero.
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
Submissions related to human medicines need to be submitted directly to the MHRA.
The approach the MHRA intends to take for products approved or pending in decentralised procedure (DCP) or mutual recognition procedures (MRP).
How to market eggs, including rules on registration, egg marking, salmonella control and egg marketing inspections in England and Wales.
How to apply for marketing authorisation via this new procedure.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Compare different evaluation approaches and choose an appropriate method.
How to renew marketing authorisations for products granted through different routes and at different times.
This guidance outlines how to create and implement a cloud strategy, and when to consider a single, hybrid or multi-cloud solution.
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. Please fill in this survey (opens in a new tab).