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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Finding the right advice and advisor is the first step in making the best decisions for your invention or business.
How to ensure the products you make or import comply with the law and are safe for consumers to use.
The Department for Business and Trade has announced the 10 SME winners of the 2024 Made in the UK, Sold to the World Awards.
Information and guidance on a range of medical devices for users and patients.
Comply with good manufacturing practice (GMP) and good distribution practice (GDP), and prepare for an inspection.
How to apply for, update and cancel licences for the manufacture, import and wholesale of human and veterinary medicines.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Marketing Authorisation Holders should review their manufacturing processes to identify and, if found, to mitigate the risk of nitrosamine impurities being present.
Anti-choking devices are intended to alleviate choking incidents after Basic Life Support protocols have been attempted and failed. There are numerous counterfeit and unbranded anti-choking devices being sold in the UK online which do not have a valid UKCA or...
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
Guidance on how to license electronic cigarettes and other inhaled nicotine-containing products (NCPs) as medicines in the UK.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
How to apply for an authorisation to manufacture authorised veterinary medicines or medicines marketed under the Exemptions for small pet animals.
Obligated packaging producers must register and meet their waste packaging recycling responsibilities.
Applications closed open for the 2018 Nuclear Decommissioning Authority (NDA) Estate Supply Chain Awards on 5 September.
Nominations are now open for the MOD Quality Awards.
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