A conceptual, stratified risk management framework is proposed that categorizes trials into low-, moderate-, and high-risk levels based on drug-related, procedural, and participant-specific variables and optimizes safety assurance in high-risk trials while avoiding the overutilization of resources in low-risk settings.
Wei Zhang, Dan-Dan Yang, Rong Shao et al.· Therapeutics and Clinical Ri...· 0 citations
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