Pharmaceutical Quality Systems
Book information
Description
When a pharmaceutical company decides to build a Quality System, it has to face the fact that there aren`t any guideline that define exactly how such a system has to be built. With terms such as quality system, quality assurance, and quality management used interchangeably, even defining the system`s objectives is a problem. This book provides a pr
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
Generics and Bioequivalence
1994 · 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 Engineering Change Control
2003 · PDF
GMP Compliance, Productivity, and Quality: Achieving Synergy in Healthcare Manufacturing
1998 · PDF