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
Learn how to publish accessible documents to meet the needs of all users under the accessibility regulations.
When and how to use the GOV.UK formats.
Adding links to content, making them accessible and GOV.UK's external linking policy.
Types of model articles of association a limited company can have, including older versions of Table A from previous company legislation.
How to write requirements for services on the Digital Outcomes and Specialists framework
This guide is intended for authors of reports commissioned by Home Office Science (HOS), research managers, editors and proofreaders. It gives…
Get help to classify textiles and which headings and codes to use.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Submission dates and how the submissions using the EC decision reliance procedure work.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to package medicines for sale and what information you must provide to consumers and healthcare professionals.
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
This guidance covers the tools and processes you need to help you write your API reference documentation
Guidelines for civil panel counsel, revised to include the new government security classifications.
Guidance on the submission, processing and assessment of all completed paediatric studies sponsored by Marketing Authorisation Holders (MAHs)
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.