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