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Jun 20, 2017 Event

4th International Conference on Clinical Trials – September 11-13, 2017

When: September 11-13, 2017


Hilton San Antonio Airport

611 NW Loop 410

San Antonio, TX 78216

Luke Stewart, Director of Product Management, will be hosting a talk.

Centralizing Data to Address Imperatives in Clinical Development

The clinical development data deluge is reaching critical mass for pharmaceuticals. Effective use of varied data for targeted outcomes remains difficult, which is especially disappointing given that more and more studies generate evidence of the risk-benefit profile of investigational products. New technologies are federating the ability to leverage analytic-ready data for innovations in clinical operations and clinical science. With the application of clinical data-as- a-service and a meta-data core, centralized clinical data lakes have the power to improve data quality, evidence generation, and time-to-insights.

Who’s Keeping Score? A Quantitative Approach to Trial Feasibility

With most trials failing to meet enrollment timelines, current approaches for feasibility are failing to identify and minimize risk. Sponsors must arm themselves with the right tools to own this analysis throughout the trial lifecycle. We will discuss a quantitative approach that operationalizes feasibility score tracking.

  • Enrollment time
    • Avoid additional trial costs
    • Ensure on-time completion
    • Mitigate trial risk
  • Patient Retention
    • Identify patient burden
    • Locate geographically convenient patients
    • Find investigators with solid patient relationships

Register Here!