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
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Guidance on the pre-application stage for Nationally Significant Infrastructure Projects.
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to meet the accommodation needs of guests, including information about gas safety and information about bills and paying rent.
Licence and registration application information for companies that deal in precursor chemicals.
Guidance on certain consultation and publicity requirements of the Nationally Significant Infrastructure Project regime.
Guidance on the pre-examination stage for Nationally Significant Infrastructure Projects.
This section details the summary report of the navigation/deck survey. It's divided by standards of training certification and watchkeeping (STCW) competence and, then by knowledge, understanding and proficiency.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
Advice for manufacturers of Class I medical devices for placing products on the UK market
Information and resources for developers about broadband infrastructure and connectivity requirements for new homes.
Rules and regulations and guidance for project qualifications.
How to write requirements for services on the Digital Outcomes and Specialists framework
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Accrediting qualifications: how and when we do it
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.