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Global Remote Clinical Trial Site Access for Monitoring and Source Data Review

Remote access to your study sites is now a requirement for continuing effective clinical operations. While COVID forced sponsors and CROs to pivot to remote site access, over 80% of sponsors and sites indicate they expect most or all of their monitoring to remain remote post COVID.

Are you prepared?

In this webinar, you will learn how leading sponsors and CROs are:

  • Enabling remote site access for monitoring and source verification.
  • Using a site-first approach to gain real-time visibility into documents and data across study sites through a single point of entry.
  • Embracing an eISF site-first approach to make sure their remote site monitoring and SDR/V strategy does not fail.