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
Guidance for legal professionals on the new rules for various areas of legal practice.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
If you're advertising or marketing, including direct marketing, you must be accurate and honest and follow the advertising codes of practice
All marketing and advertising must be: an accurate description of the…
Advertising to consumers The Consumer Protection from Unfair Trading…
There are 2 advertising codes of practice that describe how businesses…
You must describe your product accurately. This means if you make a claim…
You must check if customers want to be contacted by fax, phone, post or…
Documents on fire safety law and guidance for those who have a legal duty for fire safety in a relevant building to help them meet those duties.
What you need to know about and do to comply with the law and keep consumers safe.
Guidance on legal obligations for expert witnesses and those involved in forensic pathology investigations.
Information for competent authorities abroad (and in the UK) about obtaining evidence within the UK (or abroad) to assist in criminal investigations or proceedings.
General information including on costs assessment and remuneration for civil and crime matters.
Help your team understand why they need to meet the website and mobile app accessibility regulations.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Information to help you identify if your organisation needs to publish a modern slavery statement and best practice guidance on producing a statement.
Content directory signposting to essential guidance and resources for organisations delivering legal aid services funded by the Legal Aid Agency.
This guidance is for lawyers advising on lawfulness and legal risk in Government. It explains the common framework to assess risk across the Government Legal Profession.
Information about when you need to submit substantial amendments to a clinical trial including changes to the trial sponsor or legal representative, Investigational medicinal product certification and importation.
Directives, regulations, policies and guidance relating to the procurement of supplies, services and works for the public sector.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Guidance about expert witnesses in cases funded by legal aid, including fees, prior authority and provisions for specific types of expert.
Guidelines in Arabic, English, French, Italian, Polish, Portuguese, Spanish and Turkish to explain mutual legal assistance (MLA) and how to make a request to the UK.
Legal aid providers: find out how the LAA sets quality assurance standards and make sure you qualify.
How to comply with the requirements on promoting medicines to the public and to prescribers and suppliers of medicines.
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.