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Renew and pay for a GB or European patent online - when renewal is due, fees, renew by post or phone instead
Apply for changes to your marketing authorisation, including minor variations type IA and IB, major variations type II and extensions.
Find out about the changes if you are exporting personal protective equipment (PPE) during the coronavirus pandemic.
Find out when you must use a Defra-approved disinfectant, which product to use, and in what concentration.
Check the tariff classification for dried buffalo ears and dried beef meat scraped off from the throat, for use as animal feed.
Information about the EU Regulations and their implementation in Northern Ireland
This document explains: how patients are tested and treated, and steps in place to prevent its spread.
Pharmacovigilance system requirements
Check the regulations on aircraft parts imported with a certificate of airworthiness.
The T29 exemption allows you to treat non-hazardous pesticide washings before disposing of them to land.
Check the tariff classification for peptide nisin standardised with sodium chloride
Paper and cardboard production can cause significant pollution. This guide describes industry responsibilities for preventing pollution.
UK Health Security Agency's laboratories provide a comprehensive range of microbiological tests and services.
Find out if you need an Academic Technology Approval Scheme (ATAS) certificate to study in the UK.
When tests to detect COVID-19 are commonly used (use cases) and what to consider when deciding which type of test to employ.
The diagnosis, management and epidemiology of Bacillus spp.
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
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
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.
The UK Good Laboratory Practice Monitoring Authority (UK GLPMA) recognises that there are potential challenges COVID-19 will present to members of the GLP monitoring programme.
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