Remote monitoring of clinical trials in Trial 360

Communications
January 31, 2024

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 essential documents and focuses on compliance with the protocol by the participating research centers. Additionally, sponsors often develop their monitoring standards and practices.

¿What is remote monitoring of clinical trials?

Remote clinical trial monitoring is an innovative method that, using information technologies, allows healthcare providers, pharmaceutical companies, and clinical research organizations (CROs) to monitor the progress of clinical trials remotely without the need to conduct follow-up visits at the Center.

¿What are the advantages of remote monitoring of clinical trials?

Remote monitoring offers numerous advantages over traditional clinical trial monitoring, such as:

Operational Efficiency: Reducing costs and time by eliminating the need for frequent trips and increasing the percentage of review visits.

Instant Data Access: Real-time information for faster and more accurate decisions.

Advanced Data Security: Protecting data integrity with cutting-edge security technologies.

Collaboration without Borders: Facilitates continuous communication and early identification of challenges, promoting closer cooperation.

¿What is remote monitoring like in clinical trials at Trial 360?

In Trial 360, patient data can be viewed online, monitors can track study recruitment, compliance, and progress, and can additionally record findings and deviations. This way, researchers and sponsors/stakeholders can detect problems as they occur and react promptly. This ability to quickly identify issues is a significant advantage of remote monitoring in clinical trials in Trial 360.

Features of remote monitoring of clinical trials in Trial 360

Access to control panels with real-time updates.

Creation of users with a monitor-type role with access control by schedule.

User access configuration for a period of time with automatic inactivation of the user.

Allows recording findings and deviations and tracking them.

Monitor access in reading mode only to study patients and the designated site without the possibility of downloading documents.

Remote monitoring efficiently responds to current challenges and is a crucial step towards a more agile, patient-centered, and data-driven clinical trial model. As technology advances, we can anticipate a significant increase in adopting this approach, cultivating a path for more effective and safer clinical research.

At Integra IT, we are committed to innovation in clinical research and look forward to being part of this exciting journey towards a more efficient and results-focused future.

We invite you to review Pfizer´s expert opinion: “Federal regulations require monitoring of clinical trials,” says Lauren Litzinger, Executive Director of Global Site and Study Operations and Pfizer’s Monitoring Business Process Owner. Check the full article: Is Remote Clinical Trial Monitoring Here to Stay?

¿Questions about remote monitoring in clinical research?

Talk to our Medical Director today about remote monitoring of your clinical trial.

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