Bioequivalence assessment


The active ingredient from the pharma product and its absorption into the circulation is especially specialise in equivalence release. Bioequivalence assessment includes strategies of topical dosage forms and bio equivalence approaches for transdermal dosage form and assessment of respiratory dosage form.

  • FUNDAMENTAL BIOEQUIVALENCE ASSUMPTION
  • CRITERIA FOR BIOEQUIVALENCE
  • STUDY DESIGN
  • CONDUCT OF BIOEQUIVALENCE TRIAL

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