SOP07 - Receiving Informed Consent from Potential Participants in Clinical Research

SOP12 - Establishing Identity of Participants in Clinical Research

SOP15 - Preparing and Submitting Progress and Safety Reports for Clinical Trials of Investigational Medicinal Products (CTIMPs) and Progress Reports for Non-CTIMPs

SOP40 - Randomisation, Blinding and Code Breaking in Clinical Research

SOP59 - Reporting Breaches in Clinical Research

SOP63 - Amendments to Healthcare Research Projects