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What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Check the tariff classification for a vlogging kit with ring light made of plastics.
Find out how you could do the SFI actions for low input grassland.
Know which licence or certificate you must have to restrain, stun or kill animals which are not for human consumption, and how to carry out these operations.
Find out how you could do the SFI actions for buffer strips.
The CAT has unanimously upheld the level of penalty imposed by the CMA for a market sharing agreement relating to 20mg hydrocortisone tablets.
Guidance and support on coronavirus (COVID-19) in Scotland.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Check the tariff classification for low shoes.
Urgent public health message: UKHSA has been notified about an outbreak of food botulism in France involving a small number of British nationals.
Find out about the Sustainable Farming Incentive (SFI) actions for buffer strips, what land is eligible and what you need to do to get paid.
We handle cases relating to intellectual property disputes about: patents registered designs plant varieties If the amount sought (damages) is under £500,000 then the case can also be heard by the Intellectual Property Enterprise Court . If the amount sought...
List of Field Safety Notices from 22 to 26 April 2024.
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.
Guide for barristers asking the Law Officers for permission to join the Bar of Northern Ireland or the Faculty of Advocates in Scotland.
Check the tariff classification for bones with some meat, fat and tendons (so called soup bones).
Attorney General's jury vetting guidelines on when to use of right of stand by and what procedure to follow.
Check the tariff classification for mini-cup sets made of fine bone china.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
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