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
Information on how to gain a UK CoC for Engineering/Electro-Technical Officers or Engineering Watch Rating Certificate
Information for 16 to 19 providers delivering CDF industry placement(s) for academic year 2020 to 2021.
Guidance for organisations involved in any aspect of the pharmaceutical lifecycle or GLP studies regulated by MHRA, covering the approval of paper documents when working from home
Goods that are controlled and how to get licences for them, the UK Strategic Export Control Lists, dealing with the Export Control Organisation (ECO).
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Guide to licensing requirements and restrictions for trade control and the export of controlled military goods, software and technology.
You can use a SIEL to make shipments of specified military or dual-use items to a named consignee and/or end user.
Countries have their own rules about what goods you can bring in using an ATA Carnet. Check with the issuer in the country you’re exporting to.
How contracting authorities can find approved specialist providers and award contracts for decontamination services in relation to a CBRN or major HazMat incident.
Find out about the additional expenses rules for employees engaged on international work.
How to register your chargepoints for OZEV chargepoint grant schemes as a manufacturer.
Guidance for exporting nuclear equipment, material and technology that appears on what is known as the 'Trigger List'.
Guidance on Conditional Marketing Authorisations, exceptional circumstances Marketing Authorisations and national scientific advice
Apply for an Academic Technology Approval Scheme (ATAS) certificate, to study certain subjects in the UK.
These temporary good manufacturing practice (GMP) flexibilities will be allowed to address the current exceptional circumstances
Find registered designs in the UK
Information for companies on the import and export of controlled drugs to and from the UK.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary 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.