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Risk-Based Monitoring: A New Way to Ensure Quality Data

$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

    What started as a way to make sure data were accurate and reflected the original source, clinical trial monitoring has become time-consuming, expensive, and inefficient.
    Over the past two decades, the number and complexity of clinical trials have grown dramatically. This has created new challenges for clinical trial oversight, particularly increased variability in clinical investigator experience, site infrastructure, treatment choices…

Sidebars:
Realizing Value from Risk-based Monitoring
Risk-Based Monitoring Key Best Practices

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