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Reports, analysis and official statistics
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Data, Freedom of Information releases and corporate reports
Guidance on the decentralised and mutual recognition reliance procedure (MRDCRP) for marketing authorisation applications including information on how to apply.
Find registered patents, patent applications and pending patents
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Marburg virus is a Filovirus which, along with Ebola virus, can cause a severe and often fatal viral haemorrhagic fever (VHF).
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.
Use these forms if you import, export, or move goods through the UK.
Pharmacovigilance system requirements
Use a separate statement of objection form for each Japanese GI product name you object to.
Make sure that domains that do not send email cannot be used for spoofing.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Look up a trade mark to see if something identical or similar to your brand is already registered.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Use this form to file a translation in connection with a European patent or a European patent application
Explainer for the pharmaceutical industry on the ongoing implementation of the Veterinary Medicines Regulation relating to applications and authorisations for veterinary medicines.
The Intellectual Property Office (IPO) is the official UK government body responsible for intellectual property (IP) rights including patents, designs, trade marks and copyright. IPO is an executive agency, sponsored by the Department for Science, Innovation and Technology , supported...
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