Molins Lleonart, E. (2021). Proposing some innovative study design features to regulatory agencies (EMA and FDA) in bioequivalence trials: Reference Scaled Average Bioequivalence, and Two-Stage Adaptive Designs.
Citación estilo ChicagoMolins Lleonart, Eduard. Proposing Some Innovative Study Design Features to Regulatory Agencies (EMA and FDA) in Bioequivalence Trials: Reference Scaled Average Bioequivalence, and Two-Stage Adaptive Designs. 2021.
Cita MLAMolins Lleonart, Eduard. Proposing Some Innovative Study Design Features to Regulatory Agencies (EMA and FDA) in Bioequivalence Trials: Reference Scaled Average Bioequivalence, and Two-Stage Adaptive Designs. 2021.
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