This SOP applies to Case Report Forms (CRFs) in all types of clinical trials or studies sponsored or co-sponsored by University of Lincoln, UK and developed, supported and managed by Lincoln Clinical Trials Unit (LinCTU). This includes Clinical Trials of Investigational Medicinal Products (CTIMPs) and medical devices. The term CRF for the purposes of this document, can mean a paper CRF or electronic CRF (eCRF).
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