news roundup
ICON supported research with Carnegie Mellon University to evaluate patient-centric and patient-designed informed consent formats.
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Unlock the full potential of RBM using this new framework which integrates EDC with advanced RBM tools and goes beyond identifying risk to enable immediate action!
 Listen to this podcast to learn how
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Greenphire will participate on the SCRS Global Impact Board and work with its Leadership Council.
Read more about the exhibitors at DIA, as well as speakers, news and podcasts with DIA presenters.
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Blog Posts
Expecting transparency requirements to grow, and building anonymization options into the original processes, is the best way life sciences organizations can stay ahead of the evolving requirements and minimize their risk.
This change is likely to go into effect by the end of 2016, which means organizations that haven’t started transforming their risk monitoring process are already falling behind.
Take our survey today!
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Mobile Health
Broad consumer use of such devices is building familiarity and will facilitate the implementation of similar medical grade devices in clinical studies.
Bracket’s Patient Diary allows for clinical trial participants to record information during the trial using their smartphone.
Patient-centric technologies should focus on enhancing patient and investigator communications.
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The State of Risk-based Monitoring (RBM)
Live Webinar: Tuesday, June 21, 2016 at 11 am – 12 pm EDT
 Register Free
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Articles
Development entities that support generic drug repurposing clinical trials are either commercial or philanthropic, and primarily in the unsolved disease area.
The idea behind “adaptive” is to use data in real time to protect on-time enrollment in a constantly changing recruitment landscape.
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BIOVISUALIZATION
Effective Mining and Interpretation of Laboratory Results Data
On Demand
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