APA (7th ed.) Citation

Fernandes, E. A. F., Oudtshoorn, J. v., Tam, A., González, L. C. A., Aurela, E. G., Potthast, H., . . . Alharf, A. (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. Journal of pharmacy & pharmaceutical sciences, 27, 12398. https://doi.org/10.3389/jpps.2024.12398

Chicago Style (17th ed.) Citation

Fernandes, Eduardo Agostinho Freitas, et al. "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 27 (2024): 12398. https://doi.org/10.3389/jpps.2024.12398.

MLA (9th ed.) Citation

Fernandes, Eduardo Agostinho Freitas, et al. "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, vol. 27, 2024, p. 12398, https://doi.org/10.3389/jpps.2024.12398.