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Pain Management Modifier: Inappropriate Use of Modifiers Can Put You at Risk for Potential Fines
Date:10/28/2013

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    Other conferences of the week:

    Risk Management In Portfolio Planning For Optimal Drug Development

    This informative session is presented by expert Vladimir Shnaydman, Ph.D on Wednesday October 30, 2013, where he will provide a comprehensive view of methodology for portfolio risk analysis based on drugs interdependence and incorporation of risk mitigation strategies. He will talk in length about portfolio simulator as a prime tool for risk analysis, risk mitigation strategies at the portfolio level, and case study illustrating proposed methodology.

    Electronic Source Documents in Clinical Trials: Complying with FDA's Requirements

    This 60 minute audio session is presented by expert Dr. Mukesh Kumar on Tuesday, October 29, 2013, where he will shed light on the FDA's guidance regarding the use of electronic source documentation, providing direction to sponsors, project managers, data management centers, and clinical site staff on capturing, using, and archiving electronic data in FDA regulated clinical trials. He'll also cover the identification and specification of authorized source data originators, the creation of data element identifiers to facilitate examination of the data audit trail, capture of source data into the EDC, and Investigator responsibilities with respect to reviewing and retaining electronic data.'/>"/>

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