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 vehicle manufacturers should report CO2 emissions for their vehicles.
Submissions related to human medicines need to be submitted directly to the MHRA.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
Information about the EU Regulations and their implementation in Northern Ireland
If pharmacies wish to ‘pack down’ larger packs of a medicinal product, they need to follow these instructions
How to get scientific advice about your licence application from MHRA, including: submitting a request, your meeting with MHRA, fees.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Advice on writing clear notices and maximising replies to your FSNs.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
An overview of the work the IPO is undertaking in relation to Standard Essential Patents.
Apply to manufacture Extemporaneous preparations, Autogenous vaccines, authorisations for Equine Stem Cell Centre (ESCCA) or Non-Food Animal Blood Bank (NFABBA).
Advice for manufacturers of Class I medical devices for placing products on the UK market
Product security factsheet accompanying the Product Security and Telecommunications Infrastructure Bill, outlining the problems the Bill will address and how.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Compulsory and voluntary liquidation, the liquidation process, how liquidation affects company directors and the role of a liquidator
Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
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.
Find out if you need to use the UKCA (UK Conformity Assessed) marking on products you manufacture or handle.
Our document sets out how the new regime will deliver a range of benefits for suppliers of all sizes wishing to do business and deliver contracts for the public sector.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
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.