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Published on 21 Mar 2024

The bioequivalence study design recommendations for immediate-release solid oral dosage forms in the international pharmaceutical regulators programme participating regulators and organisations: differences and commonalities

  • Eduardo Agostinho Freitas Fernandes
  • Joy van Oudtshoorn
  • Andrew Tam
  • Liliana Carolina Arévalo González
  • Erwin Guzmán Aurela
  • Henrike Potthast
  • Katalina Mettke
  • Ryosuke Kuribayashi
  • Kohei Shimojo
  • Miho Kasuga
The bioequivalence study design recommendations for immediate-release solid oral dosage forms in the international pharmaceutical regulators programme participating regulators and organisations: differences and commonalities
Journal of Pharmacy & Pharmaceutical Sciences
doi 10.3389/jpps.2024.12398