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
This Privacy Notice explains who is processing your data, the personal data we collect, how we use it, who we share it with, and what your legal rights are.
Check the tariff classification for flavour pods.
Sets out COVID-19 testing for hospice patients and staff.
How to get fast-track approval of medical devices during COVID-19.
How to use A/B testing to evaluate your digital health product.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Configure email services securely using encryption and anti-spoofing.
How to carry out a clinical trial to apply for a marketing authorisation, manage your authorisation and report safety issues.
You can make observations on the patentability of a published patent application.
Find details of recent trade mark applications or amendments by searching the journal
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Information to help you protect, manage and enforce your intellectual property (IP) rights in the European Union and the European Economic Area (EEA).
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Applications received to amend the specification of a patent under sections 27 and 75 before the court and the Office.
Information about how to register your homeopathic medicinal product through the Simplified Homeopathic Registration Scheme or the UK Homeopathic National Rules Scheme
FCDO travel advice for St Maarten. Includes safety and security, insurance, entry requirements and legal differences.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Examples of unacceptable trade marks around protected emblems, internet domain names and your company name.
Guidance for the pharmaceutical industry on how to apply to vary a veterinary Marketing Authorisation (MA) or Homeopathic Remedy.
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.