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Register as a manufacturer, importer or distributor of active substances.
Apply for an authorisation to manufacture authorised veterinary medicines and medicines marketed under the Exemptions for Small Pet Animals.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Check the tariff classification for chewing tobacco and snuff (nasal tobacco).
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
The Renewable Transport Fuel Obligation Order regulates renewable fuels used for transport.
Paper and cardboard production can cause significant pollution. This guide describes industry responsibilities for preventing pollution.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
Check the tariff classification for flavour pods.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Find out how to export live fish, molluscs and crustaceans for farming, ornamental, or any other purpose except direct human consumption
Use a separate statement of objection form for each Japanese GI product name you object to.
Find out about Import VAT and Customs Duty when you send gifts into the UK.
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
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