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
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
How to submit an application, data package and responses for proposed or existing marketing authorisations.
How to assess household and non-household packaging from 2024 onwards if you’re a UK organisation affected by extended producer responsibility (EPR) for packaging.
How UK organisations that supply or import packaging should comply with extended producer responsibility (EPR) for packaging.
Guidance for the veterinary pharmaceutical industry on the production of mock-ups for assessment.
Service for Marketing Authorisation Holders, Manufacturers and Wholesalers.
Check the tariff classification for information displays.
Information on authorised use on goods required for drilling and production platforms on the continental shelf.
A guide for organisations interested in being an 'attribute service provider' certified against the UK digital identity and attributes trust framework.
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 and requires JavaScript).