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Recent Posts

  • Successful Split Release of Clinical Electronic Data Capture Systems (EDC)
  • Global Trial Challenge: Data Quality and Integrity
  • PROMETRIKA’s Culture of Risk Management and Inspection Readiness
  • From Envelopes to AI: The Evolution and Future of IRT in Clinical Trials
  • AI-driven Tools Enhance Data Management
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        • PRE-IND
        • IND
        • Phase 1-3
        • NDA
        • Phase 4
      • Global Capabilities
      • Protocol Development
      • Adaptive Design
      • Decentralized Clinical Trials
      • IDMC Services
      • CDISC SDTM & ADaM
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  • September 30 2017 Jennifer Yee

    The Global Library: The Benefit of Standards in a CRO-Sponsor Partnership

    The top priority of a Clinical Research Organization (CRO) is to help a sponsor conduct a successful clinical trial. That success is measured in data quality, process efficiency, and cost effectiveness.

    Continue Reading
  • August 9 2017 Stephen Cropper, MS

    The Interesting Life and Critical Role of a Clinical Research Associate (CRA)

    Clinical trials leverage the expertise of people in a wide variety of roles — researchers, project managers, clinical data managers, etc. One of the positions with which people may be less familiar is that of the clinical research associate (CRA).

    Continue Reading
  • July 14 2017 Tahmeena Chowdhury, PhD

    Individual Tumor Profiling: NCI-MATCH Clinical Trial Presents New Treatment Strategy for Patients with Cancer

    This trial is particularly interesting, given the recent US Food and Drug Administration (FDA) approval of KEYTRUDA® (pembrolizumab; Merck), the first approved cancer therapy for solid tumors based on common genetic markers as opposed to initial location of the tumors.

    Continue Reading
  • June 29 2017 Kathy Zheng, MPH

    Wearable Devices in Clinical Trials: The Current Landscape in Pharma

    Clinical research is a discipline that is constantly evolving. Currently, the most rapid innovation is occurring in the use of mobile health technology (or mHealth).

    Continue Reading
  • May 25 2017 Tahmeena Chowdhury, PhD

    Ocrelizumab: The Long Road to Approval

    In “After 40-year odyssey, first drug for aggressive MS wins FDA Approval,” (Stat News, March 28, 2017), Ron Winslow describes the fascinating journey of Roche’s new multiple sclerosis (MS) drug to obtain US Food and Drug Administration (FDA) approval.

    Continue Reading
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Recent Posts

  • Successful Split Release of Clinical Electronic Data Capture Systems (EDC)
  • Global Trial Challenge: Data Quality and Integrity
  • PROMETRIKA’s Culture of Risk Management and Inspection Readiness
  • From Envelopes to AI: The Evolution and Future of IRT in Clinical Trials
  • AI-driven Tools Enhance Data Management
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