1. Society for Clinical Data Management. (2023). Good Clinical Data Management Practices (GCDMP). Section 4.3.2, "Training," specifies that site personnel must be trained on all electronic systems used in the conduct of a clinical trial. This includes both the EDC system and any electronic source data systems, such as an EMR/EHR.
2. U.S. Food and Drug Administration. (2018). Use of Electronic Health Record Data in Clinical Investigations: Guidance for Industry. Section IV.A, "Ensuring the Quality, Reliability, and Integrity of EHR Data," states that sponsors should ensure sites have "procedures to ensure that only authorized individuals can access, create, or modify EHRs," which necessitates training on system access.
3. Løvestam, E., et al. (2017). Sourcing clinical trial data from electronic health records: a qualitative study of the process and its implications. BMC Medical Informatics and Decision Making, 17(1), 14. https://doi.org/10.1186/s12911-017-0413-y. The study highlights that a key challenge is the "need for training and support for the research nurses in how to find the data in the EHR," confirming that system access and navigation is a critical competency.