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Renew and pay for a GB or European patent online - when renewal is due, fees, renew by post or phone instead
Apply for a UK Ancestry visa if you're a Commonwealth citizen and can prove that one of your grandparents was born in the UK - eligibility, fees, documents, how to apply, how long it takes and how to settle
Pharmacovigilance system requirements
Apply for an Academic Technology Approval Scheme (ATAS) certificate, to study certain subjects in the UK.
Check how much your visa application costs in the country you’re in
Make sure that domains that do not send email cannot be used for spoofing.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
This toolkit is for Innovation Passport holders following the Innovative Licensing and Access Pathway (ILAP) and provides activities to support the design and development of medicines.
Get endorsement for the Global Talent visa to work in the UK as a digital technology expert - fintech, gaming, cyber security, artificial intelligence
Use this form to file a translation in connection with a European patent or a European patent application
Look up a trade mark to see if something identical or similar to your brand is already registered.
Visit the UK as a Standard Visitor for tourism, business, study (courses up to 6 months), medical treatment and other activities. Find out whether you need a Standard Visitor visa, or can visit without a visa.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Sets out COVID-19 testing for hospice patients and staff.
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.
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
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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