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Change your protocol, update your authorisation, report safety issues, submit safety updates and complete your end-of-trial study report.
How to apply for a clinical trial including eligibility, phases, model IMPDs, costs and how to make changes to your application.
Reports of 2 events examining how health and care data may be shared to support individual care, and the importance of understanding patient expectations.
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)’
How to notify the MHRA of your intention to carry out a clinical investigation for medical devices.
This study uses data from Young Lives Peru, a longitudinal study tracking a cohort of children from infancy to adolescence
Find out about protection for disabled people from discrimination at work, in education or dealing with the police
What you need to do to place a medical device on the Great Britain, Northern Ireland and European Union (EU) markets.
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