PhRMA Wades Into FDA Patient-Focused Data Collection: Website Systems for Crowd-Sourced Info

Trade association partners with Genetic Alliance to provide input into FDA drug development initiative. That may be an effective intervention by PhRMA as it experiments with new ways to shape regulatory policy beyond traditional advocacy efforts.

The Pharmaceutical Research & Manufacturers of America is testing an indirect, buffered system to collect and share patient-perspective data with the Food & Drug Administration.

On Nov. 4, PhRMA unveiled an effort through the DC-based Genetic Alliance to help groups representing three diseases collect patient-reported symptoms and life-impact data through web-site surveys.

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