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Following a provisional clearance in February, the CMA is now allowing the proposed deal between Arçelik and Whirlpool to go ahead.
Get help to classify plastics for import and export.
From 1 October 2024, more materials facilities will need to sample and report their waste. Sampling and reporting will be more detailed and more frequent under the amended regulations.
Business expenses you can claim if you're self-employed
Find out which gas appliances must comply with the Gas Appliances (Safety) Regulations 1995, exemption and penalties for non-compliance
Get help to classify ceramic articles for import and export.
Information about the EU Regulations and their implementation in Northern Ireland
Legal standards for labelling and composition of food products such as bottled water, milk and meat.
Advice for manufacturers of Class I medical devices for placing products on the UK market
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.
Advice on exposure to electromagnetic fields in the everyday environment, including electrical appliances in the home and mobile phones.
The rules on bringing food or animal products into Great Britain from abroad: restrictions, types of food and the amount you can bring.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
The requirements for 3D printed products will depend on whether they are classed as medical devices, personal protective equipment (PPE) or both.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Get help classifying computers, inkjet and toner cartridges and their components.
Uses of fluorinated gases (F gases) that are banned or will be banned in the future.
Check the tariff classification for a heat and moisture exchanging filter.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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