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Reference Documents

Research Governance Frameworks


European Commission Legislation


Medicines for Human Use (Clinical Trials) Regulations


Medical Devices Regulations


European Commission Clinical Trials Guidelines

For up to date European Commission guidance documents on Clinical Trials, including information on clinical trial authorisation, monitoring and pharmacovigilance, the quality of the investigational medicinal product and GCP inspections please visit the European Commission website 


International Conference on Harmonisation Guidance

University Public Statement