Article | June 23, 2020

Leveraging eRegulatory To Improve Remote Monitoring

Source: Complion

In this age of technology, every aspect of our lives is based on information and computerization. We’re constantly checking our cell phones, posting to social media platforms, or streaming news and other media. In the clinical research world, advancements in technology represent an opportunity to improve efficiency. One such example is remote monitoring which enables sponsors and CROs convenient access to site documentation.

But, remote monitoring technology initiated by sponsors can often inflict additional burden on sites, requiring them to not only print and file their regulatory documents, but scan and upload them to multiple sponsor portals, too. Fortunately, sites are beginning to identify more efficient ways to enable remote monitoring. Empowered research sites are taking control and initiating technology from their side to enhance collaboration with sponsors and streamline processes, ultimately lifting their day-to-day burden.

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