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A collection of guidance published by the CMA on markets work.
Guidelines for market investigations: their role, procedures, assessment and remedies.
Laws and regulations protecting farm animals at shows and markets, including the suitability of pens, cages or hutches
Framework for analysing government’s interaction with markets, and to understand the different ways in which government can affect markets.
Guidance on degree awarding powers, university title, designation for HEFCE funding and further education to higher education transfers.
What you need to do to comply with regulations on manufactured products you place on the market in Great Britain.
An overview of the process including submitting or fast tracking an application, naming your medicine and paying fees.
What you need to do when sheep and goats pass through your premises, including updating your holding register and reporting movements.
What you need to do to comply with regulations on manufactured goods you place on the Northern Ireland market.
What you need to do to comply with regulations on manufactured goods you place on the EU market.
The Communities and Local Government Select Committee Report on retail markets recognised the need to share good practice, and recommended that…
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
Guidance for manufacturers, their authorised representatives and importers.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
We help people, businesses and the UK economy by promoting competitive markets and tackling unfair behaviour. CMA is a non-ministerial department.
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.
The CMA consulted on a number of proposed changes to market investigations and revisions to its published guidance.
Information for manufacturers of medical devices about reporting adverse incidents and field safety corrective actions to the MHRA.
Guidance for veterinary medicines manufacturers and wholesale dealers in GB on selling and supplying products placed on the EU and UK markets before 1 January 2021 and the evidence you may need to provide.
The Capacity Market Rules provide the detail for implementing the operating framework set out in regulations.
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