Publisher
Springer Science and Business Media LLC
Subject
Pharmacology (medical),Public Health, Environmental and Occupational Health,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)
Reference65 articles.
1. WHO. Multisource (generic) pharmaceutical products:guidelines on registration requirements to establish interchangeability. Annex 6, WHO Technical Report Series, No. 1003; 2017, pp. 181–236.
2. Aitken M. Outlook for Global Medicines through 2021; 2016.
3. Cameron A, Mantel-Teeuwisse AK, Leufkens HGM, et al. Switching from originator brand medicines to generic equivalents in selected developing countries: how much could be saved? Value Heal. 2012;15:664–73.
4. Andia RAT, Barbosa T, Watanabe JH, et al. Definition and classification of generic drugs across the world. Appl Health Econ Health Policy. 2015;13:5–11.
5. Roger L, Lloyd N. Bioequivalence requirements for generic products. Pharmac Ther. 1994;62:41–55.
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