What technological options are available for ePRO data collection? How is the validity and reliability of ePRO data assessed?

Informed consent is a critical-to-quality (CTQ) factor for patient safety in clinical trials. ... informational document for study participants. Longer ... ... clinically relevant information, and organizing that information for both ... Medicine) leads ePRO clinical implementation and research. This HIV cPRO ... ... clinical trials: best practice recommendations from the ePRO consortium. Ther Innov Regul Sci, 53 (4) (2019), pp. 431-440. Crossref View in Scopus Google ... Biomedical Scientist at Department of Atomic Energy(DAE) · Experience: Department of Atomic Energy(DAE) · Location: Chengalpattu · 1 connection on LinkedIn. Dec 14, 2023 ... ... clinical trials: best practice recommendations from the ePRO Consortium. ... information underlying the analyses and findings of a clinical ... Oct 22, 2019 ... ... information to the requesting centre. Conclusion: The PITHIA trial ... (ePRO) system. Rebecca Lewis, Elizabeth Hill, Claire Snowdon, Emma ... Apr 24, 2025 ... Its primary aim is to develop and clinically assess 2 new ePRO-based palliative care interventions for adults and children, along with their ... Apr 21, 2022 ... Evidence supporting the adoption of PROMs in clinical practice. Prospective trials and population-based studies have demonstrated improved ... Jan 23, 2024 ... ... clinical trials. RELAXaHEAD clinical trials have been conducted to ... informational needs of providers along the continuum of headache ... Jun 1, 2010 ... The financial advantages of using ePRO over paper-based diaries when conducting clinical trials ... clinical information from patients.