Webinar on rSDV for Clin Ops efficiency & Cost Saving

LIVE WEBINAR
Explore rSDV for Clin Ops efficiency & Cost Saving


by
Laura LaRosa, RN MS
Quality Management Strategist &
Investigative Compliance specialist

Tuesday, 27th June
11 AM -12 Noon EST
5 PM - 6 PM CET

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Remote Source Data Verification (rSDV) Webinar

 

While on-site monitoring is one of the biggest cost drivers of clinical trial operations, Remote Source Document Verification (rSDV) offers the best alternative to significantly reduce onsite monitoring activities to build efficiencies, data quality and assure human subject protection.

This webinar will explore the differences between rSDV and other monitoring methods, how to maintain subject privacy in the process of collecting source documents and what 21 CFR Part 11 requires, strategies for remote review of source documents at sites that do not utilize electronic medical records. Explore the great benefits of rSDV and for the types of studies it can be leveraged in a big way.

This webinar covers:

  • Remote Source Document Verification (rSDV) process
  • Strategies & challenges in implementing rSDV
  • Benefits of rSDV
  • Subject confidentiality & 21 CFR Part 11 requirements
  • CRA compliance in remote setting