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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)’
Investors and businesses may be legally required to tell the government about certain sensitive acquisitions under the National Security and Investment Act.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
How to register your medical devices with the Medicines and Healthcare products Regulatory Agency (MHRA) for the markets in Great Britain and Northern Ireland
What you need to know before you can place a medical device on the Great Britain market with a UKCA mark.
Directory of current ICH Guidelines which have been implemented by the Medicines and Healthcare products Regulatory Agency.
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Information on how to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
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