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Sample size determination in bioequivalence studies using statistical assurance.

Arne RingB LangC KazarohoDetlew LabesRobert SchallHelmut Schütz
Published in: British journal of clinical pharmacology (2019)
The advantage of deriving the assurance for BE trials is that uncertainty is directly expressed as a parameter of variability.
Keyphrases
  • quality control
  • solid phase extraction
  • case control
  • molecularly imprinted
  • high resolution