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When you must report the amount of electrical and electronic equipment (EEE) you place on the market and how to do it.
Waste electrical and electronic equipment (WEEE) - retailer and wholesaler responsibilities, waste collection and compliance schemes.
Find out which regulations apply to your products and where to go for further information on how to comply with them.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
How to transport electrical and electronic waste materials, such as small household appliances, IT equipment and power tools (note 26).
Reports for the amount of EEE placed on the market and WEEE collected in the UK under the WEEE Regulations.
Get help to classify drones and aircraft parts for import and export.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
Get help to classify various types of vehicles such as mobility scooters, dumpers and utility vehicles, all-terrain vehicles and e-bikes for import and export.
Check the tariff classification for four-wheeled vehicles powered by an electric motor fitted with a hydraulic lifting device and telescopic jib.
Guide to licensing procedure and other restrictions for export of controlled dual-use items, software and technology, goods for torture and radioactive sources.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
Minimum technical specification for manufacturers of chargepoint units for residential properties covered by OZEV chargepoint grant schemes.
Guidance for manufacturers, their authorised representatives and importers.
Minimum technical specification for manufacturers of chargepoint units for commercial properties covered by OZEV chargepoint grant schemes.
The rules for manufacturing mercury added products in Great Britain, as well as importing and exporting them between Great Britain and non-EU countries.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
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