SCRS Talks podcast series

‘SCRS Talks’ to Rick Arlow about quality regulatory work during a pandemic

Joe Wochna Clinical Research Trends, eRegulatory, Remote Monitoring

In terms of the service a research site provides to the sponsor of a study, regulatory work is of utmost importance. Regulatory teams are burdened with figuring out how to make sure this critical work is done even when all the parties involved in the study are not in the same room. This is particularly true during this pandemic. So how do regulatory teams provide the highest quality especially during this time?

Society for Clinical Research Sites (SCRS) sought the answer to that question in a recent episode of the organization’s “SCRS Talks” podcast series when they interviewed Complion CEO Rick Arlow.

Source document review

3 requirements for a remote SDR/SDV solution

Joe Wochna Remote Monitoring, SDR/SDV

During this pandemic, a key aspect of remote monitoring that seems to be a source of struggle for the industry is SDR/SDV. This is an extremely extremely risky aspect as sensitive PHI is shared across virtual organizational walls. Fortunately, there is a very simple solution if the right eRegulatory solution is used. This blog post takes a look at the three primary requirements when looking for a remote SDR solution.

Remote monitoring

Leveraging eRegulatory to Improve Remote Monitoring

Joe Wochna eRegulatory, Remote Monitoring

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.