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
What denatured alcohol is, and how you apply for authorisation to produce, stock, distribute, sell or use it.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
For MAHs, manufacturers, wholesalers, retailers (including vets) and feed businesses on the manufacture and movement of veterinary medicines in relation to the NI Protocol and Brexit.
Registers of authorised manufacturers, wholesale dealer sites and retailers.
This report provides a review of literature and evidence on long lasting insecticide treated nets and private sector
This notice is about the production, distribution or use of denatured alcohol in the UK. Denatured alcohol is alcohol that has been made unsuitable for drinking by the addition of denaturants.
Register as a manufacturer, importer or distributor of active substances.
Waste electrical and electronic equipment (WEEE) - retailer and wholesaler responsibilities, waste collection and compliance schemes.
Guidance for the pharmaceutical industry on who can be a Marketing Authorisation Holder, named distributor or local representative and how to make changes to these.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Details of the exceptions to copyright that allow limited use of copyright works without the permission of the copyright owner.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
The Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP) Consultative Committee discusses the manufacture and wholesale distribution of medicines.
What you need to know about and do to comply with the law and keep consumers safe.
If you put EEE on the UK market you must follow rules on both the EEE you sell and the EEE that becomes waste (WEEE).
Guidance for manufacturers and distributors of premixtures and feedingstuffs containing veterinary medicines or specified feed additives.
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.