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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.
How to market eggs, including rules on registration, egg marking, salmonella control and egg marketing inspections in England and Wales.
The EU Emissions Trading System Union Registry: how it works, how Kyoto units are used for compliance within the EU ETS and how to participate in carbon allowance auctions.
Model byelaw set for local authorities to regulate the use of markets.
If the UKCA marking applies to products you manufacture or supply, you will have specific obligations and responsibilities for compliance, depending on your role.
Provides a conceptual framework within which evidence on market definition can be organised, and discusses practical issues that may arise.
How to make sure that your products are properly checked for conformity and your technical documents are managed correctly.
Guidance for manufacturers, their authorised representatives and importers.
Summaries of the CMA’s recommendations to government, industry, regulators and others relating to markets work.
One of the key issues that has been identified as crucial to the viability and success of the retail market is the way in which the market itself…
OIM report suggests trade between UK nations is not a challenge for most, while policy design can minimise disruption.
Guidance on the approach to ensure that instruments placed on the market conform to the Measuring Instruments Directive.
Information about what to do if you receive a warning or advisory letter from the CMA.
A new pathway supporting innovative approaches to the safe, timely and efficient development of medicines to improve patient access.
How to get help researching export markets and sign up for seminars on exporting.
Explains the changes introduced by the Enterprise and Regulatory Reform Act 2013 to the conduct of market studies and market investigations by the CMA under the Enterprise Act 2002, as amended.
The CMA has outlined 3 key risks to effective competition on AI Foundation Models and has set out plans for further action in the market.
Advice for manufacturers of Class I medical devices for placing products on the UK market
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