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
a MHRA Regulating Medicines and Medical Devices Safety Guidelines for Magnetic Resonance Imaging Equipment in Clinical Use November 2014 Medicines and Healthcare Products Regulatory Agency eee Acknowledgements The following are acknowledged for their contribution to this document BAMRR BIR MR committee British Chapter ISMRM HSE IPEM MR SIG Metrasens Ltd SCoR Siemens Philips Medical GE Medical S Keevil T Gilk T O Woods Mr D Grainger Medici