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 outcomes digitally using devices such as smartphones, tablets, or computers. Electronic patient-reported outcomes (ePRO) is an innovative tool that transforms how data is collected and analyzed in clinical trials. … Continue reading What is ePRO, Electronic Patient-Reported Outcome?
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 Clinical Outcome Assessment) uses electronic tools and technologies to collect and evaluate patient outcome data in clinical trials and clinical research. It allows… Continue reading Electronic Clinical Outcome Assessment (eCOA): What is and Who Uses it?
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. However, effective financial administration is often overlooked. Amidst the complexity of clinical trials and scientific quests, diligent planning, implementation, and recording systems are crucial, piling… Continue reading Clinical Invoicing Software: A Practical Walkthrough with Trial360
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, offering practical solutions to streamline operations and enhance outcomes. Find out multiple benefits of this transformative software, from reducing administrative burdens to improving collaboration. With integrated systems covering… Continue reading Efficiency in execution of research protocols
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, safety, and effectiveness. What is quality control in clinical research? Quality control is the set of procedures and activities carried out to ensure that the data… Continue reading How to Ensure Quality Control in Clinical Research?
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 study team and site, and compromise future submissions. Patient reporting adherence facilitates the early identification of symptoms and risk factors, prevents dropouts,… Continue reading Adherence Reporting in Vaccine Trials: [+98% Adherence Rates]
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 preventive actions to be identified, reviewed, reported, and taken appropriately to ensure patient safety and maintain data integrity. What are deviations from the protocol? According to ICH E3 guidelines,… Continue reading Findings and Deviations in Trial 360
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 audit trail for all actions performed within the system in which a study is being conducted. Here we share the key requirements you must have… Continue reading What are the requirements of Audit Trail in CFR 21 Part 11?
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 regulation requires monitoring of clinical trials to ensure the accuracy and reliability of the data generated by the trial. Monitoring includes reviewing data and… Continue reading Remote monitoring of clinical trials in Trial 360
Research sites face a critical challenge that has an effect on their sustainability and overall performance: invoicing and financial management. It is common for sites either to lack a specialized billing system or to have one that is not connected to their day-to-day activities. The billing method vary according to the type of contract,… Continue reading Financial Management in Research Sites: Key to Sustainability
Integra IT.
For Sites.
Other Solutions.
For CROs.
About us.
