Describe the role of ePROs in patient safety How can ePROs be used in post-marketing surveillance of drugs?

Apr 6, 2023 ... The rollout of electronic PRO (ePRO) will also bring great promise for the application of PROs in clinical trials, streamlining the information ... Mar 25, 2020 ... Eligible patients received detailed information regarding the study and, if interested, were ... measures: ISPOR ePRO Good Research Practices Task ... Oct 22, 2019 ... ... information to the requesting centre. Conclusion: The PITHIA trial ... (ePRO) system. Rebecca Lewis, Elizabeth Hill, Claire Snowdon, Emma ... eCOA and ePRO · Electronic Data Capture (EDC) · Decentralized Clinical Trials ... Informative Pages. Cookie Policy · Privacy Policy · Privacy Policy for ... Informed consent is a critical-to-quality (CTQ) factor for patient safety in clinical trials. ... informational document for study participants. Longer ... ePRO are patient-provided information about symptoms, side effects, drug timing and other questions recorded on an electronic device during a clinical trial. A Bayesian group sequential design for randomized biosimilar clinical trials with adaptive information borrowing from historical data. Watch Video Session ... Nov 17, 2023 ... Information about clinical trials is often scattered across various sources, making it challenging for potential participants to find relevant ... Feb 20, 2025 ... Section 2.10 states that “All clinical trial information should be recorded, ... electronically: The past, present, and promise of ePRO ... more information, a project collaborator will meet the patient ... this trial, future clinical trials could build on this result not by asking whether the ABM is ...