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Are You Properly Equipped to Execute Risk-Based Site Monitoring?

$30.00

Copyright: This PDF purchase is for a Single user for review or filing purposes only. The PDF is watermarked. If you are interested in a PDF reprint to post on your website or distribute electronically, or hard-copy reprints, please contact Marah Walsh at mwalsh@pharmavoice.com.

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Product Description

As the life-science industry focuses on moving toward a risk-based site monitoring approach where partial source document verification (SDV) is employed, it is critical that the clinical organization have the right tools and processes in place to efficiently execute such a strategy. As is typical with the implementation of any new process, some sponsors and CROs have struggled with their initial venture into the new risk-based site monitoring paradigm. The specific reasons vary, but a key shortcoming is the lack of proper tools to support the planning…

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