Redefining the Relationship Between Sponsors/CROs and Clinical Research Sites

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Continuing to build on a legacy of innovation, Signant’s Virtual Site Monitoring offers a novel solution to decades-old challenges related to clinical research site management during clinical trials.

Qualifying, initiating, and monitoring sites used to involve a heavy travel burden for CRAs and substantial budget allocation on the part of sponsors or CROs.

Now, these burdens can be eliminated all together by leveraging this truly unique solution, which offers CRAs and stakeholders a way to see exactly what an on-site study monitor sees in real-time, live, first person video.

Learn how this solution will redefine clinical site monitoring not just in the era of an active pandemic but into the future.

Originally published in InSite Journal Fall 2021 issue.

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