Textbooks - BS Publication

Reference Books
Environmental Monitoring
for Cleanrooms and
Controlled Environments
Anne Marie Dixon
2007 978-0824723590
256 pages £ 115.00
Supramolecular Chemistry -
Fundamentals and
Applications:
Advanced Textbook
Katsuhiko Ariga and Toyoki
Kunitake
2007 978-3540012986
208 pages TBA
Reagent Chemicals
Specifications and
Procedures, 10th Ed.
American Chemical Society Specifications
2006 0-8412-3945-2
806 pages $ 189.50
Mass Spectroscopy : A Textbook
NEW
Jurgen H. Gross
Contents : 1. Introduction 2. Gas Phase Ion Chemistry 3. Isotopes 4. Instrumentation 5. Electron Ionization
6. Fragmentation of Organic Ions and Interpretation of EI Mass Spectra 7. Chemical Ionization 8. Field Ionization and Field
Desorption 9. Fast Atom Bombardment 10. Matrix-Assisted Laser Desorption/Ionization 11. Electrospray Ionization
12. Hyphenated Methods
2007 3-540-40739-1 536 pages Rs. 1495.00
21 st Century Pharmaceutical Development
Peter Blaisdell
Name Reactions, 2nd Ed.
A Collection of Detailed Reaction
Mechanisms, More than
300 reactions
NEW
Jie Jack Li
2007 3-540-40203-9
465 pages Rs. 1495.00
Contents : 1. Financing Strategies for Small Drug Developers 2. Managing Basic Research in the Twenty-First
Century 3. Protecting Intellectual Property in the New Millennium 4. The Marketing of Pharmaceutical Products
5. Regulatory Affairs in the Twenty-First Century 6. Regulatory Affairs in the Twenty-First Century 7. Advances in
Preclinical Toxicology Studies for Pharmaceutics 8. Drug Product Formulation Development 9. Twenty-First Century
Manufacturing 10. The Art (and Science) of Developing a Clinical Strategy 11. The Role of Statistics in Drug Development
12. Project Management in Drug Development 13. Outsourcing in Pharmaceutical Development
Indian Rpt. 2004 388 pages Rs. 4495.00
Validation of Active Pharmaceutical Ingredients, 2nd Ed.
Ira R. Berry and Daniel Harpaz
Contents : 1. Introduction 2. The Legal Framework for the Regulation of Active Pharmaceutical Ingredients 3. The Legal
Basis for Validation 4. Drug Master Files 5. The FDA’s Perspectives on Active Pharmaceutical Ingredient Manufacturing,
cGMP Controls, and Validation 6. Domestic and Foreign API Manufacturing Facility Audits and Findings 7. Validation of
APIs : A Case Study 8. Active Pharmaceutical Ingredient Validation : An Overview and Comparative Analysis 9.
Impurities in Drug Substances and Drug Products 10. Investigating Process Deviations 11. Technology Transfer : Active
Pharmaceutical Ingredients 12. Postapproval Changes to Bulk Drug Substances 13. Vendor Qualification and Certification
14. Quality Assurance Systems 15. Cleaning for Active Pharmaceutical Ingredient Manufacturing Facilities 16. Validation
of Sterile APIs 17. Validation of Biotechnology Active Pharmaceutical Ingredients 18. Microbiological Attributes of Active
Pharmaceutical Ingredients 19. Excipients : Facility, Equipment, and Processing Changes 20. API Terminology and
Documentation
Indian Rpt. 2004 588 pages Rs. 4995.00
8 Price are subject to change without priour notice
Pharma Book Syndicate