What should sponsors do to prepare for ePRO audits?

Evaluating Risk in the Era of Decentralized Clinical Trials - By Allison ... October 25, 2023 Applied Clinical Trials SCOPE Europe 2023 Roundtable: eCOA- and ePRO ... ACCME's informational and educational materials inform CME stakeholders, the ... Outline for the Self-Study for ACCME Reaccreditation for the March, July & ... Dec 14, 2023 ... ... clinical trials: best practice recommendations from the ePRO Consortium. ... information underlying the analyses and findings of a clinical ... treatment with improvements obtained in earlier clinical trials. A ... Paper presented at the Drug Information Association Conference on Benefits and Challenges. Aug 3, 2023 ... ... ePRO, and eCOA solutions. ... clinical trial conduct by streamlining trial management and providing mobile access to essential information. Feb 7, 2018 ... based guidance on PRO-specific information that should be in- cluded in clinical trial protocols. ... ePRO Good Research Practices Task Force ... 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 ... Aug 28, 2023 ... Consent to Participate: Informed consent was obtained from all individual participants included in the study. Copyright information. © 2023 The ... Jul 29, 2022 ... In clinical trials, the most common IoT devices are electronic Clinical Outcome Assessments (eCOA) or Patient Report Assessments (ePRO), sensors ... Dec 4, 2020 ... ... research question (their demographic information is ... Recommendations for best practice ePRO implementation in oncology clinical trials.