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Guidance for the pharmaceutical industry on how to apply for an authorisation to place a veterinary medicine on the UK market or part of, or to expire one.
Explainer on product information templates to be used by applicants and Marketing Authorisation Holders (MAHs) of veterinary medicines.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Legal terms for veterinary medicines, marketing of non-medicinal products including medicinal words and phrases, how to complain.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
Check the tariff classification for dried buffalo ears and dried beef meat scraped off from the throat, for use as animal feed.
Pharmacovigilance system requirements
Check the regulations on aircraft parts imported with a certificate of airworthiness.
Use this form to file a translation in connection with a European patent or a European patent application
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
Make sure that domains that do not send email cannot be used for spoofing.
Use an OGEL to export controlled dual-use or military goods, software and technology overseas.
Volume 20 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
Check the tariff classification for peptide nisin standardised with sodium chloride
Check the tariff classification for flavour pods.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
Volume 52 of the non-technical summaries granted under the Animals (Scientific Procedures) Act 1986 during 2013.
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