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
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Protocols and procedures for testing the distinctiveness, uniformity and stability (DUS) of certain agricultural and vegetable plants.
What you need to do to work and operate in the aviation industry.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
Information to help you protect, manage and enforce your intellectual property (IP) rights in China.
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
his page provides practical information to help you make the most of your IP when doing Business in Chile.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
This guide provides information about being arrested in Germany and what conditions are like in prison there.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
Advice for medical professionals to follow when assessing drivers with neurological disorders.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
Class and permitted use of passenger ships, cargo ships, tankers, tugs, tenders, fishing boats, yachts, commercial vessels, and the required certificates.
How contracting authorities can find approved specialist providers and award contracts for decontamination services in relation to a CBRN or major HazMat incident.
Guidance for exporting nuclear equipment, material and technology that appears on what is known as the 'Trigger List'.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Use a global project licence to simplify the export of military goods and technology classed as collaborative defence projects.
This page provides practical information to help you make the most of your IP when doing business in Peru.
How end-use controls apply to weapons of mass destruction (WMD) related goods, software, technology and technical assistance.
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.