Guidance on preparing an application to MHRA Medicines for a

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1. Guidance on preparing an application to MHRA Medicines for a

Integrated Research Application System IRAS Guidance on preparing an application to MHRA Medicines for a Clinical Trial Authorisation using IRAS Clinical trial authorisation CTA is required for any clinical trial of an investigational medicinal product CTIMP to be conducted in the UK The standard application for CTA is the European Commission application form available from the EudraCT website at http eudract emea europa eu The whole of the EudraCT dataset is availa
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