New Edition Coming Soon! Handbook of Bioequivalence Testing, Second Edition

BOCA RATON, Fla. - Aug. 21, 2014 - PRLog -- 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. In addition, advances in the analytical technology used to detect drug and metabolite levels have made bioequivalence testing more difficult to conduct and summarize. The second edition of this book has been completely updated to include the most current information available, including new findings in drug delivery and dosage form design and revised worldwide regulatory requirements.

Features
- Serves as a state-of-the-art global reference on bioequivalence testing

- Includes details on novel delivery systems as well as CAM and biological products

- Offers insight on choosing contract research organizations and managing global trials

- Discusses the importance of establishing GCP / GLP compliant systems (effective lab and clinical practice)

- Provides a brief review of emerging trends in bioequivalence testing and dissolution and disintegration testing methodologies

- Includes a glossary of terms

Pre-order your copy now and SAVE 25% when you enter promo code CMN55 at checkout here: http://www.crcpress.com/product/isbn/9781482226379