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Detailed guidance, regulations and rules
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Data, Freedom of Information releases and corporate reports
A collection of guidance published by the CMA on markets work.
Quality and labelling rules for growing, packing, distributing, importing and selling fresh fruit and vegetables.
Laws and regulations protecting farm animals at shows and markets, including the suitability of pens, cages or hutches
The topics in the Market Guidance are based on analysis of the notifications received under the NSI Act and feedback from stakeholders on their experience of the system.
The Capacity Market Rules provide the detail for implementing the operating framework set out in regulations.
Comprehensive review to radically improve access to financial advice to benefit all consumers.
The Communities and Local Government Select Committee Report on retail markets recognised the need to share good practice, and recommended that…
Guidance on degree awarding powers, university title, designation for HEFCE funding and further education to higher education transfers.
CMA publishes report and proposed principles following review of foundation models
Guidelines for market investigations: their role, procedures, assessment and remedies.
VAT treatment of transactions in commodities, commodity derivatives and on terminal markets.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
Understand and avoid all types of anti-competitive and cartel activity including price-fixing, collusion, bid-ridding and sharing markets. Know how to report concerns to the CMA.
Sources of advice and financial support for UK farmers exporting agricultural products to the EU and beyond
Find out the rules on investments using open market price rules and how you can charge for your services as an ISA manager.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
Information for consumers and businesses on their rights and responsibilities under consumer law.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
How to use early market engagement to help you write clearer requirements.
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