1. Ministry of Health, Labour and Welfare. Guideline for Bioequivalence Studies of Generic Products. 2012. Available at: https://www.nihs.go.jp/drug/be-guide(e)/Generic/GL-E_120229_BE_rev140409.pdf. Accessed 14 Jun 2020.
2. Ministry of Health, Labour and Welfare. Guideline for Bioequivalence Studies for Different Strengths of Oral Solid Dosage Forms. 2012. Available at: https://www.nihs.go.jp/drug/be-guide(e)/strength/GL-E_120229_ganryo.pdf. Accessed 14 Jun 2020.
3. Ministry of Health, Labour and Welfare. Guideline for Bioequivalence Studies for Formulation Changes of Oral Solid Dosage Forms. 2012. Available at: https://www.nihs.go.jp/drug/be-guide(e)/form/GL-E_120229_shohou.pdf. Accessed 14 Jun 2020.
4. Ministry of Health, Labour and Welfare. Guideline for Bioequivalence Studies for Different Oral Solid Dosage Forms. 2012. Available at: https://www.nihs.go.jp/drug/be-guide(e)/GL-E_120229_zaikei.pdf. Accessed 14 Jun 2020.
5. Ministry of Health, Labour and Welfare. Guideline for Bioequivalence Studies of Generic Products Q&A. 2012. Available at: https://www.nihs.go.jp/drug/be-guide(e)/Generic/QA-E_120229_BE.pdf. Accessed 14 Jun 2020.