Top 5 Benefits of Automation in Clinical Trials
Curious about the benefits of automation in clinical trials? Discover how it can enhance data accuracy, efficiency, and improve patient engagement.
Navigating the Complex World of Clinical Trials for Medical Devices
Facing challenges with clinical trials for medical devices? Explore key insights on regulations, trial design, and how to navigate this process.
Enhancing Patient Tracking with Technology
How can technology improve patient tracking in clinical trials? Explore the benefits of real-time monitoring and better patient engagement.
Finding the Right Sponsor for Your Clinical Trial
Want to find the right clinical trial sponsors to support your research and studies? Learn some useful tips and tricks in this guide.
Digital Transformation: Harnessing eSource in Clinical Trials
The pharmaceutical industry is undergoing a significant shift towards digital transformation, and clinical trials are no exception. One of the key drivers of this transformation is the adoption of eSource, electronic data capture, and other digital technologies. This blog will explore the benefits and challenges of harnessing eSource in clinical trials and how it can…
Remote Monitoring in Clinical Trials: A Comprehensive Overview
Clinical trials are the backbone of medical research, enabling the development of new treatments, medications, and medical devices. However, conducting clinical trials can be a complex, time-consuming, and costly process. Remote monitoring has emerged as a game-changer in clinical trials, revolutionizing the way data is collected, monitored, and managed. In this blog post, we’ll explore…
Insights into Remote Clinical Trial Monitoring Practices
The clinical trial landscape is undergoing a significant transformation, driven by technological advancements, regulatory changes, and the need for more efficient and patient-centric approaches. Remote monitoring clinical trial practices have emerged as a crucial aspect of this transformation, offering a new paradigm for conducting clinical research. In this blog, we’ll delve into the insights of…
A Comprehensive Guide to Developing a Clinical Research Training Program Checklist
Training is often considered a prerequisite and one of the essential components of clinical research. With proper training, researchers understand all the ethical implications of the study and stay compliant with all the regulations throughout the study. To that end, the training aims to teach the researchers about all the steps of the research, from…
Understanding sIRBs and Why Your Research Needs One
sIRBs multi-site research Historically, research organizations and sites have relied on the institutional review board (IRB) and its oversight. sIRBs multi-site research is an important characteristic today. These committees are usually locally managed by the research institutions themselves, but in some cases, the organization also chooses independently administered IRBs. Recently, there has been a change…
Predictive Analytics and Automation: The Future of Clinical Trial Monitoring
With automation and artificial intelligence, clinical trial teams can recruit and retain more patients. Plus, predictive analytics allow clinical trial teams to make better predictions, and therefore, better decisions about patient behavior — this way, they can reach out before a study ends. Currently, AI and predictive analytics can benefit clinical trial monitoring and clinical…