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Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Look up a trade mark to see if something identical or similar to your brand is already registered.
Get help to classify pharmaceutical products used to treat or prevent diseases or ailments (in humans or animals), including comparators used in clinical trials and placebos.
Guidance on Animal Test Certificates (ATCs) required to carry out the field trial of a veterinary medicine in animals (clinical trial) in the UK.
Check the tariff classification for flavour pods.
How to use A/B testing to evaluate your digital health product.
Reclaim VAT you've paid on goods and services bought in the UK to use in your business if you’re registered as a business outside the UK.
Explainer for the pharmaceutical industry on the implementation of the Veterinary Medicines Regulation relating to Pharmacovigilance.
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 an OGEL to export controlled dual-use or military goods, software and technology overseas.
Use this form to transform your Madrid Protocol Designation to a UK Trade Mark application.
Check the tariff classification for surface-active preparation for washing the skin and the hair (gel 2-in-1).
Use form C88 (status) as proof of authorisation to import or export for the country of destination.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Information and guidance on a range of medical devices for users and patients.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
How to spot Aujeszky’s disease, what to do if you suspect it and measures to prevent its spread.
You must include the appropriate legal basis for your application when you apply to MHRA for a marketing authorisation.
Volume 53 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Monitor the progress of a patent application through search reports, open to the public inspection files, and caveats.
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