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Data, Freedom of Information releases and corporate reports
How to use and supply animal by-products (ABPs) as farm animal feed or in feed, and how to get your site registered and approved.
Find out about the long-term effects some people can have after having COVID-19.
Substances that are classed as persistent organic pollutants (POPs) and when you're allowed to use them.
Covering thalidomide, lenalidomide, and pomalidomide: temporary guidance for pregnancy prevention arrangements for patients taking them during COVID-19
It's illegal to drive if you're unfit to do so because you're on legal or illegal drugs, or you have certain levels of drugs or medicine in your blood
These reports explain our assessment of the scientific evidence used to lead to regulatory decisions on the safety of medicines or medicines classes.
FCDO travel advice for Bolivia. Includes safety and security, insurance, entry requirements and legal differences.
Guidance for the pharmaceutical industry on Marketing Authorisations for veterinary medicines.
Find out about the symptoms of COVID-19, what to do if you or your child has them and when to get medical help.
Find out if the goods you're declaring to inward or outward processing are classed as sensitive goods.
How to use a cost utility analysis to evaluate your digital health product.
How to use a cost benefit analysis to evaluate your digital health product.
Information for patients, healthcare professionals and developers of new medicines
Buy or get someone's permission to use a patent, trade mark, design or work under copyright
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
The carnivores you can feed, when your site must be registered, authorised, or recognised, and the animal by-products you can use.
How to use a cost effectiveness analysis to evaluate your digital health product.
This series brings together all documents relating to Energy Consumption in the UK
How the MHRA makes decisions on when a product is a medical device (borderline products), and which risk class should apply to a medical device.
How to register as a producer, and the rules you must follow to produce and market bottled drinking water.
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