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How to conform with the legal requirements for placing medical devices on the market.
Animal by-products (ABPs) you can use to make pet food, how to provide samples, and how to package your products.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to get a parallel import licence for your medicine in the UK, including pharmacovigilance requirements and submitting your application.
Providing vital research into COVID-19 immunity and vaccine effectiveness nationally.
This paper analyses implications for inflation, output and the exchange rate in the presence of domestic and external shocks
Public health advice for prisons and other prescribed places of detention.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Find out how to apply VAT zero rating for the supply of those plants and seeds that are used to grow food for human consumption.
The T32 exemption allows you to treat non-hazardous pesticide washings in a biobed or biofilter.
How a marketing authorisation holder should report a defect with a veterinary medicine.
The diagnosis, management, surveillance and epidemiology of syphilis.
Information about the EU Regulations and their implementation in Northern Ireland
Licences and authorisations to import genetic material, research and diagnostic samples, trade samples and display items, and some live animals and animal products.
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