Electronic Clinical Outcome Assessment (eCOA): What is and Who Uses it?

Electronic Clinical Outcome Assessment (eCOA) A New Era in Clinical Research

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?

Clinical Invoicing Software: A Practical Walkthrough with Trial360

Billing for clinical protocols

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

Efficiency in execution of research protocols

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, 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

Quality control in clinical research

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, 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 Quality control in clinical research

Leveraging Technology to Elevate Patient Reporting Adherence in Vaccine Clinical Trials: Reaching +98% Adherence Rates

Leveraging Technology to Elevate Patient Reporting

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 Leveraging Technology to Elevate Patient Reporting Adherence in Vaccine Clinical Trials: Reaching +98% Adherence Rates

Findings and Deviations in Trial 360

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 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

What are the requirements of Audit Trail in CRF 21 Part 11?

What are the requirements of Audit Trail in CRF 21 Part 11

In the 21 CRF 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 CRF 21 Part 11?

Remote monitoring of clinical trials in Trial 360

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 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

Financial Management in Research Sites: Key to Sustainability

Financial Management in Research Sites Key to Sustainability

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

Four Benefits of Having a Smart Scheduling System in Sites

Four Benefits of Having a Smart Scheduling System in Sites

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 the success of the study. Using an intelligent scheduling system can bring great advantages to the research team, among them: Reduction of protocol deviations Thanks… Continue reading Four Benefits of Having a Smart Scheduling System in Sites