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PRA ‘toolkit’ pinpoints rare-disease clinical trial risks The free Patient-Centric Trial Development Toolkit is aimed toward helping sites and sponsors identify and minimize risks in rare-disease clinical studies. PRA Health Sciences has launched its Patient-Centric Trial Development Toolkit, a resource designed to aid clinical trial teams in identifying risks that could stymie the effectiveness and efficiency of their research, and deal with those problems. Outsourcing-Pharma recently spoke with Scott Schleibner, senior vice president of the Center for Rare Diseases at PRA Health Sciences, about the toolkit, the unique challenges rare disease studies face, the importance of patient-centric trials, and more.

Scott schleibnerCentric trial development toolkitPra health sciencesRapid participation burden survey toolHealth sciencesPatient centric trial development toolkitRare diseasesCentric protocol risk assessment toolParticipation burden survey toolInvolvement dossierRare disease patientsClinical developmentPatient centricityClinical evolutionData managementPhasei ii