Webinar on rSDV for Clin Ops efficiency & Cost Saving

rSDV offers the best alternative option to altogether reduce onsite monitoring activities, 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.

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Explore rSDV for Clin Ops efficiency & Cost Saving
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
About Our Speaker
 Laura LaRosa, RN MS
 Quality Management Strategist &
 Investigative Compliance specialist
 Date & Time: Tuesday, 27th June 2017 , 11 AM -12 Noon EST | 5 PM - 6 PM CET
Register here: https://www.makrocare.com/webinar-registration-onexplore-rsdv-for-clin-ops-efficiency-cost-saving

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