https://www.selleckchem.com/pr....oducts/bms-986365.ht
Coordination with the central institutional review board will expedite the approval process. Protocol adherence, adverse event monitoring, and data collection and export can be facilitated by building electronic health record processes, though implementation can start using traditional clinical trial tools. Lastly, establishment of a centralized institutional process optimizes coordination of COVID-19 studies. Implementation of the REMAP-COVID trial within a large US healthcare system is feasible and facilitated by multidisciplinary
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