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Find out which regulations apply to your products and where to go for further information on how to comply with them.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Apply to become or identify an approved manufacturer authorised to carry out conformity assessment.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guidance for manufacturers, authorised representatives, and responsible persons.
Lists of standards that businesses can use to show their products, services or processes comply with essential requirements of legislation.
Guidance for manufacturers, importers and distributors.
The ETL (or Energy Technology Product List, ETPL) is a government list of energy-efficient plant and machinery.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
How to register your chargepoints for OZEV chargepoint grant schemes as a manufacturer.
We are allowing alternative courses of actions for manufacturing or laboratory equipment during the outbreak.
This notice explains when protective equipment is zero-rated and children's car seats and travel systems are reduced-rated at 5% VAT.
If you put EEE on the UK market you must follow rules on both the EEE you sell and the EEE that becomes waste (WEEE).
Resources for business.
There are different regulations which apply to devices and equipment including hand gels and PPE (personal protective equipment)
Waste electrical and electronic equipment (WEEE) - retailer and wholesaler responsibilities, waste collection and compliance schemes.
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