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Regulatory requirements

Shifting the Paradigm to Pragmatic Evidence Generation

Hayleigh Culliton2023-12-12T10:00:06-05:00December 12th, 2023|Categories: Blog|Tags: comparative effectiveness, Cost-effective research, Data automation, Evidence generation platforms, Evidence generation strategy, evidence-based medicine, Health technology assessment, Healthcare decision-making, Healthcare research automation, Integrated evidence generation, Medical data integration, Pharmaceutical Industry, Post-marketing studies, Pragmatic evidence generation, Regulatory requirements, Technology-driven research|

By: Richard Gliklich, MD, OM1 & Sonja Wustrack, MPH, OM1 Integrated Evidence Generation Integrated evidence generation (IEG) is a framework [...]