Table of Contents In a world where it seems everyone is talking about artificial intelligence, and its numerous benefits, we cannot ignore the fact that artificial intelligence is transforming industries and sectors all over the world and one of them is the pharmaceutical area. Essentially, AI is a robust tool helping to overcome large problems… Continue reading How Artificial Intelligence is Transforming Clinical Trials: The Case of AstraZeneca
Table of Contents What is eConsent and How Does it Improve Clinical Trials? We all recognize the vital role informed consent plays in clinical trials. These trials operate under a complex set of regulations governing how consent is obtained. It is estimated that eConsent implementation in clinical trials reduce the time spent on consent-related tasks… Continue reading eConsent Software for Optimal Clinical Trials
Table of Contents This blog provides the immense potential of CRISPR, a revolutionary genome editing tool that is revolutionizing the field of DNA editing. What is CRISPR? CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) is a gene-editing technology that allows scientists to modify DNA sequences with high precision and efficiency. It is based on a… Continue reading CRISPR: The Promise of Gene Editing in Clinical Trials
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 deadlines, extensive planning, and assessments are tasks that impact the point-of-care services and staff workload. A software tool like Trial360, which includes an integrated scheduling system, can… Continue reading Scheduling at Research Sites: From a Problem to an Opportunity
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]
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