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How a product complies with EU safety, health and environmental requirements, and how to place a CE marking on your product.
RA1, RA2, RA3, RA4, RA5 bilingual forms for completion following a drugs test in custody.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
The landing obligation (‘discard ban’) applies to quota species and is being phased in over the period 2015 to 2019.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Information for manufacturers of medical devices on post-market surveillance, reporting adverse incidents and field safety corrective actions to the MHRA.
Guidance for manufacturers, importers and distributors.
Information about the MHRA regulates medical devices in Northern Ireland and what legislation applies to manufacturers and suppliers.
A wholesale dealer in Great Britain may import Qualified Person certified medicines from the European Economic Area if certain checks are made by the ‘Responsible Person (import)’
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