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Community Registry Grows Research Abilities Of Pulmonary Fibrosis Foundation
Clinical Research News | In July, the Pulmonary Fibrosis Foundation (PFF) launched the PFF Community Registry to begin collecting data directly from patients in the U.S. with pulmonary fibrosis (PF) and interstitial lung disease (ILD)—together with their nonprofessional caregivers and biological family members—as well as lung transplant recipients previously diagnosed with PF or ILD.
Sep 21, 2022
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3 Ways to Communicate Your Value to Trial Participants
Clinical Research News | Although we’re seeing an increasing trend of site networks and academic research centers insourcing technology solutions themselves, unless they’re offered an Adaptive Experience that lets them choose how they want to participate at every step of the trial, they aren’t given a choice about using the technology. Keeping technology top of mind is critically important for research solutions to succeed.
Sep 16, 2022