Automated Clinical Trial Monitoring Workflows Make a Lean Team More Efficient

Clinical trials are a critical part of the drug development process, but they can be complex and time-consuming to manage. One of the biggest challenges facing clinical trial teams is the need to manually create and track documents, such as reports, confirmation letters, and follow-up letters. This can be a major drain on resources, taking clinical research associates (CRAs) away from more important tasks, such as site monitoring.

Enterin faced this challenge firsthand. Until 2019, their clinical monitoring team was manually creating reports and letters, which took 5-6 hours per week away from site monitoring. They also had to manually track site visits on a spreadsheet.

To improve efficiency, Enterin implemented an automated clinical trial monitoring solution. This solution automates the creation of letters and reports, automatically notifies CRAs and other stakeholders when site visits are due, and makes it easier to share data with senior leadership and site managers.

As a result of this automation, Enterin's clinical monitoring team has saved 5-6 hours per week. This has allowed them to focus on more important tasks, such as site monitoring. Additionally, the solution has improved communication and collaboration between the clinical monitoring team and other stakeholders.

In this case study, we will learn more about the challenges that Enterin faced, the solutions they implemented, and the benefits they have realized. We will also discuss the importance of automation in clinical trial monitoring and how it can help organizations to improve efficiency, accuracy, and compliance.

If you are looking for ways to improve the efficiency, accuracy, and compliance of your clinical trial monitoring workflows, automation is a great option. Contact us today to learn more about how we can help you.