Andres Felipe Pineda Torres Scheduling at Research Sites: From a Problem to an Opportunity Daily site operations and visit scheduling are often a burden for clinical research teams, who constantly seek to engage and build long-term relationships with participants. Dealing with tight deadlin... Resources Trial 360 Mar 29, 2024
Andres Felipe Pineda Torres What is ePRO, Electronic Patient-Reported Outcome? What is electronic patient-reported outcomes (ePRO)? ePRO stands for " Electronic Patient-Reported Outcomes. " It is a tool that allows patients to record electronically and submit their health outcom... Resources TrialPal Mar 21, 2024
Andres Felipe Pineda Torres Electronic Clinical Outcome Assessment (eCOA): What is and Who Uses it? Table of Contents The global eCOA market is poised for significant growth in the coming years. Grand View Research shows the market is expected to reach $20.5 billion by 2028. eCOA (electronic Clinica... Resources TrialPal Mar 14, 2024
Andres Felipe Pineda Torres Clinical Invoicing Software: A Practical Walkthrough with Trial360 How is the billing of clinical protocols in Trial360? In the world of clinical research studies, a key focus is on precision, compliance with regulations, and maintaining ethical principles. Howeve... Resources Trial 360 Mar 6, 2024
Andres Felipe Pineda Torres Efficiency in execution of research protocols Welcome to the forefront of efficiency in research protocols execution! Protocol research centers struggle with balancing quality and affordability. Trial360 emerges as a beacon of innovation, offerin... Resources Trial 360 Feb 27, 2024
Andres Felipe Pineda Torres How to Ensure Quality Control in Clinical Research? To establish confidence in the results of clinical research, quality control in the execution of the protocol is an essential pillar. Quality control must guarantee the research results' integrity, sa... Resources Trial 360 Feb 23, 2024
Andres Felipe Pineda Torres Adherence Reporting in Vaccine Trials: [+98% Adherence Rates] Poor patient reporting adherence can prolong the trial duration by increasing the time required to gather complete and accurate data. This can extend the overall cost of the trial while burdening the ... Resources TrialPal Feb 16, 2024
Andres Felipe Pineda Torres Findings and Deviations in Trial 360 Clinical research protocols are carried out following the International Council for Harmonization (ICH) guidance on Good Clinical Practice (GCP), which outlines the requirements for corrective and pre... Resources Trial 360 Feb 7, 2024
Andres Felipe Pineda Torres What are the requirements of Audit Trail in CFR 21 Part 11? In the 21 CFR Part 11, the FDA established guidelines for electronic records and electronic signatures. A fundamental aspect of compliance in clinical trials is maintaining a secure and comprehensive ... Resources Trial 360 Feb 6, 2024
Andres Felipe Pineda Torres Remote monitoring of clinical trials in Trial 360 Remote monitoring of clinical trials in Trial 360: Innovation for a More Efficient and Safe Future Clinical trials are vital in developing and approving new drugs, treatments, and medical devices. The... Resources Trial 360 Jan 31, 2024
Andres Felipe Pineda Torres Scheduling in Research Sites (4 Key Benefits). Scheduling at research sites is not as straightforward as in other clinical services. Commonly, patient visits must be scheduled according to a research protocol and their compliance is essential for ... Resources Trial 360 Jan 26, 2024
Andres Felipe Pineda Torres A Compliant and Easy to Setup Delegation Log with Trial360 Delegation Log in Clinical Trials Trial360 delegation log is a vital tool for research sites. It serves several crucial purposes, ensuring compliance, accountability, and efficient study conduct. Get ... Resources Trial 360 Jan 17, 2024
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