Generics and Bioequivalence
Book information
Description
Published in 1994: This text focuses on the determination of bioequivalence between formulations that are pharmaceutically equivalent and manufactured using acceptable chemistry, manufacturing and controls and in accordance with Good Manufacturing Practices.
Similar books
GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers, (Volume 2 - Regulations, Standards, and Guidelines): Regulations, Standards, and Guidelines
2004 · PDF
Pharmaceutical Water: System Design, Operation, and Validation, Second Edition
2010 · PDF
Validating Pharmaceutical Systems: Good Computer Practice in Life Science Manufacturing
2005 · PDF
Quality and GMP Auditing: Clear and Simple
1997 · PDF
Planar Chromatography - Mass Spectrometry
2015 · PDF
Pharmaceutical Quality Systems
2000 · PDF
Pharmaceutical Engineering Change Control
2003 · PDF
GMP Compliance, Productivity, and Quality: Achieving Synergy in Healthcare Manufacturing
1998 · PDF