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The Competition and Markets Authority (CMA) has completed its remittal into the private healthcare market and has brought article 22 of the 2014 Order into force.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
The eMIT provides information about prices and usage for generic drugs and pharmaceutical products.
The orders provide measures on benefits, incentive schemes and better information for patients.
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
This is a summary of how Monitor, the Office of Fair Trading and the Competition Commission assess proposed mergers involving NHS hospitals.
Guidance for industry on flexible approaches to regulation we are taking during the COVID-19 outbreak.
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