Quantification of sofosbuvir and ledipasvir in human plasma by UPLC–MS/MS method: Application to fasting and fed bioequivalence studies
Tài liệu tham khảo
Rezk, 2016, Biomed. Chromatogr.
Website, http://apps.who.int/prequal/info_applicants/BE/2015/Sofosbuvir_BE25March2015.pdf (accessed 18.06.15.)
FDA, Guidance for industry: bioanalytical method validation. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER), Center for Veterinary Medicine (CV) (2001).