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Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
Guidance for manufacturers, importers and distributors.
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
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)’
RA1, RA2, RA3, RA4, RA5 bilingual forms for completion following a drugs test in custody.
How to register your medical devices with the MHRA for the markets in Great Britain and Northern Ireland.
Information for entertainers and musicians, from non-visa national countries, such as EU Member States and the US, visiting the UK for performance and work.
What you need to do before your product can be placed on the Great Britain market with a UKCA mark.
The information required by the Regulator of Social Housing and the deadlines for submission.
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