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Reference Books cGMP Current Good Manufacturing Practices for Pharmaceuticals Manohar A. Potdar Contents : 1. Personnel 2. Surroundings, Buildings and Facilities 3. Equipment 4. Materials Management 5. Quality Management 6. Manufacturing Operations and Control 7. Documentation and Records 8. Pharmaceutical Validation 9. Out Sourcing 10. Post Operational Activities 11. Sterile Pharmaceutical Products 12. Site and Plant Security 13. Safety and Environmental Protection 14. Good Pharmaceutical Wholesaling Practices 15. Pharmaceutical Audit 2008 978-81-88449-53-9 828 pages HB Rs. 1495.00 Liquid Chromatography- Mass Spectrometry, 3rd Ed. Wilfried M.A. Niessen Contents : 1. INTRODUCTION 2. Liquid Chromatography and Sample Pretreatment 3. Mass Spectrometry 4. TECHNOLOGY 5. Strategies in LC-MS Interfacing 6. History of LC-MS Interfaces 7. Interfaces for Atmospheric- Pressure Ionization 8. Atmospheric-Pressure Ionization 9. APPLICATIONS: SMALL MOLECULES 10. LC-MS Analysis of Pesticides 11. Environmental Applications of LC-MS 12. LC-MS in Drug Discovery and Development 13. LC-MS in Drug Metabolism 14. Quantitative Bioanalysis Using LC-MS 15. Clinical Applications of LC-MS 16. LC-MS Analysis of Steroids 17. LC-MS in Food Safety Analysis 18. LC-MS Analysis of Plant Phenols 19. APPLICATIONS: BIOMOLECULES 20. LC- MS analysis of Proteins 21. LC-MS analysis of Peptides / Enabling Technology 22. LC-MS in proteomics 23. LC-MS for identification of post-translational modifications 24. LC-MS analysis of oligosaccharides 25. LC-MS analysis of lipids and phospholipids 26. LC-MS analysis of nucleic acids 2006 0824740823 608 pages £ 99.00 Pharmaceutical Chemical Analysis : Methods for Identification and Limit Tests Ole Pedersen Contents : Part I Identifications 1. Precipitation in Identification 2. Color Reactions in Identifications 3. Tests Part II Limit Tests 4. Precipitation in Limit Tests 5. Color Reactions in Limit Tests 6. Tests 2006 0-8493-1978-1 157 pages £ 99.00 Six Sigma in the Pharmaceutical Industry Nunnally NEW Contents : 1. The Enormous Initial Mistake 2. The Origins of Six Sigma 3. Evolution 4. Revolution 5. Paradox 6. Action and Reaction 7. Close Enough : ... Or On Target 8. Make More ... Foster ! 9. Case Studies 10. The Camera Always Lies 11. Keeping It Simple 12. Why use Control Charts 13. Average and Range Control Charts 14. Origins and Theory 15. Charts for Individuals 16. Practical Considerations 17. Improving Laboratories 2007 1-4200-5439-2 204 pages £ 49.99 Structure-based Drug Discovery Harren Jhoti and Andrew R. Leach NEW NEW Contents : 1. Five Years of Increasing Structural Biology Throughput - A Retrospective Analysis 2. Protein Production for Structural Genomics - Strategies for the Next Phase 3. Introduction to Fragment Screening 4. Fragment-based NMR Screening in Lead Discovery 5. Fragment-based Screening by X-ray Crystallography 6. Scaffold-based Drug Discovery 7. Biophysical Methods : Mechanism of Action Studies 8. Illustration of Current Challenges in Molecular Docking : An Application of Docking, and Virtual Screening to Thymidine Kinase 9. Scoring Functions : From Freeenergies of Binding to Enrichment in Virtual Screening 2007 978-1-4020-4406-9 249 pages Euro. 129.95 6 Price are subject to change without priour notice Pharma Book Syndicate
Statistical Design and Analysis of Stability Studies Shein-Chung Chow Contents : 1. Introduction 2. Accelerated Testing 3. Expiration Dating period 4. Stability Designs 5. Stability Analysis with Fixed Batches 6. Stability Analysis with Random Batches 7. Stability Analysis with a Mixed Effect Model 8. Stability Analysis with Discrete Responses 9. Stability Analysis with Multiple Components 10. Stability Analysis with Frozen Drug Products 11. Stability Testing for Dissolution 12. Current Issues and Recent Developments 2007 1-58488-905-5 330 pages £ 49.99 Microencapsulation Methods and Industrial Applications, 2nd Ed. (Drugs and the Pharmaceutical Sciences Vol. 158) Benita Simon Contents : 1. Biodegradable Microsphere : Advances in Production Technology 2. Advances in the Technology for Controlled Release Pesticide Formulations 3. Multiparticulate Pulsatile Drug Delivery for Parenteral Depot Systems and their Application in the Pharmaceutical Industry 5. Coupling Methods to Obtain Ligand-Targeted Liposomes and Nanoparticles 6. Industrial Technologies and Scale up 7 Evaluation and Characterization of Micro- and Nanoparticulate Drug Delivery Systems. Drug Release from Microparticulate Systems. 2006 0-8247-2317-1 756 pages Rs. 2495.00 Computer Aided Drug Design : Methods and Applications Thomas J.Perun C.L.Propst Pharma Book Syndicate Price are subject to change without priour notice NEW Contentes : 1. Introduction to Computer-Aided Drug Design 2. Uses of Computer Graphics in Computer-Aided Drug Design 3. Theoretical Aspects of Drug Design : Molecular Mechanics and Molecular Dynamics 4. X-Ray Crystallography and Drug Design 4. Approaches to Drug Design Using Nuclear Magnetic Resonance Spectroscopy 6. Enzyme Kinetics in Drug Design : Implications of Multiple Forms of Enzymes on Substrate and Inhibitor Structure-Activity Correlations 7. Computer- Aided Design and Evaluation of Angiotensin-Converting Enzyme Inhibitors 8. Role of Computer-Aided Molecular Modeling in the Design of Novel Inhibitors of Renin 9. Inhibitors of Dihydrofolate Reductase 10. Approaches to Antiviral Drug Design 11. Conformation Biological Activity Relationships for Receptor-Selective, Conformationally Constrained Opioid Peptides 12. Design of Conformationally Restricted Cyclopeptides for the Inhibition of Cholate Uptake of Hepatocytes. Rpt. 2007 Rs. 1295.00 Solvent Recovery Handbook, 2nd Ed. Ian M Smallwood Contents : 1. Introduction 2. Removal of solvents from air 3. Separation of solvents from water 4. Solvent recovery equipment 5. Separation of solvents from residues 6. Separation of used solvents 7. Drying solvents 8. Used solvent disposal 9. Good operating procedure 10. Choice of solvent with recovery in mind 11. Improvements in batch distillation 12. Extractive distillation 13. Significance of solvent properties 14. Recovery notes 15. Properties of solvent pairs 16. Properties of individual solvents 2002 0-63205-647-9 432 pages Rs. 1495.00 International Stability Testing David J. Mazzo Contents : The ICH Stability Guideline; David J. Mazzo –Photostability Testing; Terry G. Beaumont – The ICH Stability Guideline for Biological and Biotechnological Products; Manfred Haase – Stress Testing Program : Drug Substance Characterization Studies; Elisabeth Pacaud – Statistical and Regulatory Aspects of Drug Stability Studies : An FDA Perspective; William R. Fairweather, Tsae-Yun Daphne Lin – Matrixing and Bracketing Designs for Stability Studies : An Overview from the European Perspective; Per Helboe – Assessment of Preservative Activity During Stability Sutdies; Norman Hodges – Drug Substance Solid-State Characterization and Stability; Ivan Santos – Variations and Changes in Europe; Stability Requirements; Anthony C. Cartwright Postapproval FDA Stability Requirements ; Dhiren N. Shah – Current Application in Japan of the ICH Stability Guidelines : Does Japanese Registration Require More Than Others Do ?; Sumie Yoshioka – Stability Testing for Australia; Susan Walters – The WHO Stability Guideline; Sabine Kopp-Kubel Manuel Zahn – Stability Testing Considerations for Some Non-ICH Areas; Terry G. Beaumont Indian Rpt. 2004 352 pages Rs. 4495.00 Reference Books 7
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