 Pharmaceutical Manufacturing Handbook: Regulations and Quality
ISBN: 978-0-470-25959-7
Hardcover
856 pages
March 2008
US $195.00
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PREFACE.
SECTION 1 GOOD MANUFACTURING PRACTICES (GMP) AND OTHER FDA GUIDELINES.
1.1 Good Manufacturing Practices (GMPs) and Related FDA Guidelines (James R. Harris).
1.2 Enforcement of Current Good Manufacturing Practices (Kenneth J. Nolan).
1.3 Scale-Up and Postapproal Changes (SUPAC) Regulations (Puneet Sharma, Srinivas Ganta, and Sanjay Garg).
1.4 GMP-Compliant Propagation of Human Multipotent Mesenchymal Stromal Cells (Eva Rohde, Katharina Schallmoser, Christina Bartmann, Andreas Reinisch, and Dirk Strunk).
SECTION 2 INTERNATIONAL REGULATIONS OF GOOD MANUFACTURING PRACTICES.
2.1 National GMP Regulations and Codes and international GMP Guides and Guildelines: Correspondences and Differences (Marko Närhi and Katrina Nordström).
SECTION 3 QUALITY.
3.1 Analytical and Computational Methods and Examples for Designing and Controlling total Quality Management Pharmaceutical Manufacturing systems (Paul G. Ranky, Gregory N. Ranky, Richard G. Ranky, and Ashley John).
3.2 Role of Quality Systems and Audits in Phatmaceutical Manufacturing Environment (Evan B. Siegel and James M. Barquest).
3.3 Creating and Managing a Quality Management system (Edward R. Arling, Michelle E. Dowling, and Paul A. Frankel).
3.4 Quality process improement (Jyh-hone Wang).
SECTION 4 PROCESS ANALYTICAL TECHNOLOGY (PAT).
4.1 Case for Process Analytical Technology: Regulatory and Industrial Perspectives (Robert P. Cogdill).
4.2 Process Analytical Technology (Michel Ulmschneider, Yves Roggo).
4.3 Chemical imaging and Chemometrics: Useful Tools for Process Analytical Technology (Yves Roggo and Michel Ulmschneider).
SECTION 5 PERSONNEL.
5.1 Personnel Training in Pharmaceutical Manufacturing (David A. Gallup, Katherine V. Domenick, and Marge Gillis).
SECTION 6 CONTAMINATION AND CONTAMINATION CONTROL.
6.1 Origin of Contamination (Denise Bohrer).
6.2 Quantitation of Markers for Gram-Negatie and Gram-Positive Endotoxins in Work Enironment and as Contaminants in Pharmaceutical Products Using Gas Chromatography–Tandem Mass Spectrometry (Alvin Fox).
6.3 Microbiology of Nonsterile Pharmaceutical Manufacturing (Ranga Velagaleti).
SECTION 7 DRUG STABILITY.
7.1 Stability and Shelf Life of Pharmaceutical Products (Ranga Velagaleti).
7.2 Drug Stability (Nazario D. Ramirez-Beltran, Harry Rodriguez, and L. Antonio Estévez).
7.3 Effect of Packaging on Stability of Drugs and Drug Products (Emmanvel O. Akala).
7.4 Pharmaceutical Product Stability (Andrew A. Webster).
7.5 Alternative Accelerated Methods for Studying Drug Stability: Variable-Parameter Kinetics (Giuseppe Alibrandi).
SECTION 8 VALIDATION.
8.1 Analytical Method Validation: Principles and Practices (Chung Chow Chan).
8.2 Method Validation and Quality Assurance (Isabel Taverniers, Erik Van Bockstaele, and Marc De Loose).
8.3 Validation of Laboratory Instruments (Herman Lam).
8.4 Pharmaceutical Manufacturing Validation Principles (E. B. Souto T. Vasconcelos D. C. Ferreira, and B. Sarmento).
Index.
