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How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Pharmacovigilance system requirements
When and how you need to register your item or apply for an exemption certificate to deal in ivory.
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...
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Information about the EU Regulations and their implementation in Northern Ireland
AVU provides services for genotypic antiviral resistance testing of HIV and HCV, investigation of HIV transmission events and HSV antiviral resistance testing by phenotyping.
Check the tariff classification for flavour pods.
Information to help you protect, manage and enforce your intellectual property (IP) rights in Colombia.
What you need to do to work and operate in the aviation industry.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Guidance to help organisations choose a monitoring approach for stack emissions to air that meets Environment Agency and MCERTS requirements (formerly part of M2).
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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.
Information on how to revalidate a UK CoC (and UK GMDSS at the same time).
Apply to become or identify an approved manufacturer authorised to carry out conformity assessment.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
This guidance outlines the requirements for claiming preferential tariffs under the Developing Countries Trading Scheme (DCTS).
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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