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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.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
An overview of the process including submitting or fast-tracking an application, naming your medicine and paying fees.
Information for people who wish to apply to release a vaccine or a blood product to market in the UK.
Promotes policies and practices that improve privately delivered health care for the poor in low and middle-income countries.
The orders provide measures on benefits, incentive schemes and better information for patients.
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