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Advice for manufacturers of Class I medical devices for placing products on the UK market
Application form RX2 for an order that a restriction be disapplied or modified.
The start of an anti-dumping investigation covering monosodium glutamate from China.
The Advisory Committee on Releases to the Environment examines how EU law on genetically modified products applies in modern plant breeding.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Modified materials for the 2023 phonics screening check.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
How to conform with the legal requirements for placing medical devices on the market.
Details of consent for Cambridge University Crop Science Centre to release genetically modified organisms, reference 21/R54/01.
We give statutory advice to ministers on the risks to human health and the environment from the release of genetically modified organisms (GMOs). ACRE is an advisory non-departmental public body, sponsored by the Department for Environment, Food & Rural Affairs...
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