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remote monitoring clinical trials covid

3 Reasons Principal Investigators Need eSource
Running a Site 3 Minute Read

Building Better Oversight – 3 Reasons Principal Investigators Need eSource

What’s wrong with the way that most sites have been recording data for decades? While much of research data is still being collected on paper, digital adoption across source, regulatory and remote monitoring is rapidly increasing among sponsors, CROs, and research sites. Many of the challenges that Principal Investigators (PIs) face during the conduct of...

Running a Study
3 Minute Read -

This is Why Remote Monitoring in Clinical Trials is Slower Than Expected

Most clinical trials are conducted with onsite monitoring, where a clinical research assistant (CRA) visits the site to perform source data verification, drug accountability, and other review functions. As COVID has imposed significant travel restrictions and stay at home mandates, many CRAs cannot currently perform on-site visits; even if they could, many of their sites...

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