How are errors in ePRO data detected?

Feb 6, 2018 ... ... information that should be included in clinical trial protocols. It ... ePRO Good Research Practices Task Force report. Value Health ... May 15, 2023 ... The US Food and Drug Administration has made it clear that electronic capture of clinical trial source data is preferred over paper-based data ... Jan 1, 2022 ... Clinical trials need to reach a representative patient population ... patients with an onslaught of information or technical terms. Feb 20, 2025 ... Section 2.10 states that “All clinical trial information should be recorded, ... electronically: The past, present, and promise of ePRO ... Oct 23, 2023 ... ... information in the informed consent process about the ... clinical trials: best practice recommendations from the ePRO consortium. ... ePRO at home are needed but cannot be provided like in the clinical setting. ... Communicating quality of life information to cancer patients: a study of six ... May 27, 2024 ... ... information in clinical trials, the potential for identifying influential factors on patients' QOL ... ePRO measurement in clinical trials. Clinical Data Acquisition Standards Harmonization Implementation Guide for Human Clinical Trials Version 2.1 (Final) Prepared by the CDISC CDASH Team Notes ... Mar 27, 2023 ... Designed to enhance communication between clinicians and patients in diverse research and clinical settings; Created to be relevant across ... ... patient needs, leading to improved patient engagement and more reliable trial results. As part of our unified clinical research information software, it ...