Rick Liwski

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creating collaborations with regulators patient advocacy groups & the regulated pharmaceutical industry accelerated development of safer new medical products faster safer smarter medical product development public private partnership research services drug development clinical trials biomarkers regulatory science patient advocacy rare diseases alzheimers disease parkinsons disease duchenne muscular dystrophy safety biomarkers clinical outcome assessments patient-reported outcomes neuroscience research biotech collaboration fda endorsement ema qualification clinical trial design data sharing model-based simulations translational medicine therapeutic innovations evidence-based medicine predictive analytics orphan disease therapies data management clinical trial optimization real-world data patient safety medical product evaluation therapeutic areas risk assessment regulatory pathways preclinical development standardized assessments collaborative networks public-private partnerships healthcare outcomes neonatal drug development treatment efficacy clinical trial enrichment tools data repositories biostatistics data analytics patient engagement scientific leadership global health initiatives therapeutic efficacy healthcare innovations chronic disease management health care health wellness & fitness hospital & health care information technology & services enterprise software enterprises computer software b2b