eCOA/ePRO 2017

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The biopharma industry overwhelmingly relies upon paper forms when collecting clinical outcomes data. Though this is a time-tested and familiar technique, it carries the risk of delivering compromised, or otherwise unusable data. The transition to e-Patient Reported Outcomes and e-Clinical Outcomes Assessment techniques can eliminate these data quality challenges.

At CBI’s eCOA/ePRO 2017, experts in clinical operations and outcomes research pinpoint the best ways to overcome logistical and organizational obstacles and speed up the adoption of far more efficient technology.

Date: December 13-14, 2017
Location: Philadelphia, PA
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