APA (7th ed.) Citation

Kanfer, I., & Shargel, L. (2008). Generic drug product development: International regulatory requirements for bioequivalence. Informa Healthcare.

Chicago Style (17th ed.) Citation

Kanfer, Isadore, and Leon Shargel. Generic Drug Product Development: International Regulatory Requirements for Bioequivalence. New York: Informa Healthcare, 2008.

MLA (9th ed.) Citation

Kanfer, Isadore, and Leon Shargel. Generic Drug Product Development: International Regulatory Requirements for Bioequivalence. Informa Healthcare, 2008.