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Data availability The trial sponsor (Eli Lilly and Company) participated in the design and execution of the study, as well as collection, management, analysis and interpretation of the data
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These have more obvious safety and efficacy data.
Alternately, FDA should consider restricting imports to bulk manufacturers whose DMFs were included in ANDA applications and subsequently reviewed beyond just the completeness step
Researchers note that the consistency of effects across multiple substances and outcomes provides a strong rationale for dedicated clinical trials
