Handbook of Bioequivalence Testing

by Sarfaraz K. Niazi

As the generic pharmaceutical industry continues to grow and thrive, so does the need to conduct efficient and successful bioequivalence studies. In recent years, there have been significant changes to the statistical models for evaluating bioequivalence, and advances in the analytical technology used to detect drug and metabolite levels have made bioequivalence testing more difficult to conduct and summarize. The Handbook of Bioequivalence Testing offers a complete description of every aspect of bioequivalence testing.

550 pages, Hardcover

Published August 22, 2007

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[Hoa Ha Phuoc]

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