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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.
How to choose data tools and infrastructure that are flexible, scalable, sustainable and secure.
Development of a standard approach for AI and autonomy in networked multi-sensor systems in security and defence.
The requirements for packaging DNLEU
Publish your code and use open source to improve transparency, flexibility and accountability.
Look up a trade mark to see if something identical or similar to your brand is already registered.
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
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Your purchasing strategy must show you’ve considered commercial and technology aspects, and contractual limitations.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
How to get fast-track approval of medical devices during COVID-19.
Understand how to manage a project which uses artificial intelligence.
How to apply for an exemption to use a restricted substance to manufacture electrical and electronic equipment.
Calculate value build-up costs for use with the Single Administrative Document (SAD) using form C89.
Examples of how and when to adjust the customs value for commercial level and quantity when using Methods 2 or 3 if you’re an importer or clearing agent.
Using recommended patterns for workplace wifi networks and sharing infrastructure.
Information on how to gain a UK CoC for Engineering/Electro-Technical Officers or Engineering Watch Rating Certificate
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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