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Tuesday, July 29, 2008
SATU
      1. UV and IR Spectra: Pharmaceutical Substances (UV and IR) and Pharmaceutical and Cosmetic Excipients (IR). R.M. Muller 2002
      2. Analytical Profiles of Drug Substances, Vol 01. Klaus Florey 1972
      3. Analytical Profiles of Drug Substances, Vol 02. Klaus Florey 1973
      4. Analytical Profiles of Drug Substances, Vol 03. Klaus Florey 1974
      5. Analytical Profiles of Drug Substances, Vol 04. Klaus Florey 1975
      6. Analytical Profiles of Drug Substances, Vol 05. Klaus Florey 1976
      7. Analytical Profiles of Drug Substances, Vol 06. Klaus Florey 1977
      8. Analytical Profiles of Drug Substances, Vol 07. Klaus Florey 1978
      9. Analytical Profiles of Drug Substances, Vol 08. Klaus Florey 1979
      10. Analytical Profiles of Drug Substances, Vol 09. Klaus Florey 1980
      11. Analytical Profiles of Drug Substances, Vol 10. Klaus Florey 1981
      12. Analytical Profiles of Drug Substances, Vol 11. Klaus Florey 1982
      13. Analytical Profiles of Drug Substances, Vol 12. Klaus Florey 1983
      14. Analytical Profiles of Drug Substances, Vol 13. Klaus Florey 1984
      15. Analytical Profiles of Drug Substances, Vol 14. Klaus Florey 1985
      16. Analytical Profiles of Drug Substances, Vol 15. Klaus Florey 1986
      17. Analytical Profiles of Drug Substances, Vol 16. Klaus Florey 1987
      18. Analytical Profiles of Drug Substances, Vol 17. Klaus Florey 1988
      19. Analytical Profiles of Drug Substances, Vol 18. Klaus Florey 1989
      20. Analytical Profiles of Drug Substances, Vol 19. Klaus Florey 1990
      21. Analytical Profiles of Drug Substances, Vol 20. Klaus Florey 1991
      22. Analytical Profiles of Drug Substances, Vol 21. Harry G. Brittain 1992
      23. Analytical Profiles of Drug Substances, Vol 22. Harry G. Brittain 1993
      24. Analytical Profiles of Drug Substances, Vol 23. Harry G. Brittain 1994
      25. Analytical Profiles of Drug Substances and Excipients, Vol 24. Harry G. Brittain, 1996
      26. Analytical Profiles of Drug Substances and Excipients, Vol 25. Harry G. Brittain, 1998
      27. Analytical Profiles of Drug Substances and Excipients, Vol 26. Harry G. Brittain 1999
      28. Analytical Profiles of Drug Substances and Excipients, Vol 29. Harry G. Brittain 2002
      29. Profiles of Drug Substances, Excipients and Related Methodology, Vol 30. Harry G. Brittain 2003
      30. Profiles of Drug Substances, Excipients and Related Methodology, Vol 31. Harry G. Brittain 2004
      31. Profiles of Drug Substances, Excipients and Related Methodology, Vol 33. Harry G. Brittain 2007
      32. Instrumental Data for Drug Analysis, 3rd Ed-Vol 1. Terry Mills III 2006
      33. Instrumental Data for Drug Analysis, 3rd Ed-Vol 2. Terry Mills III 2006
      34. Instrumental Data for Drug Analysis, 3rd Ed-Vol 3. Terry Mills III 2006
      35. Instrumental Data for Drug Analysis, 3rd Ed-Vol 4. Terry Mills III 2006
      36. Instrumental Data for Drug Analysis, 3rd Ed-Vol 5. Terry Mills III 2006
      37. Instrumental Data for Drug Analysis, 3rd Ed-Vol 6. Terry Mills III 2006
      38. HPLC Methods for Pharmaceutical Analysis, Volume 1. George Lunn 1997
      39. HPLC Methods for Pharmaceutical Analysis, Volumes 2-4. George Lunn 2000
      40. HPLC Methods for Recently Approved Pharmaceuticals. George Lunn 2005
      41. A Compendium of Unofficial Methods for Rapid Screening of Pharmaceuticals by Thin-Layer Chromatography. FDA Division of Testing and Applied Analytical Development
      42. A Practical Handbook of Preparative HPLC. Dr. Donald A. Wellings 2006
      43. A Primer for Sampling Solids, Liquids, and Gases: Based on the Seven Sampling Errors of Pierre Gy . Patricia L. Smith 2001
      44. Acidic and Basic Reagents. Hans J. Reich 1999.
      45. Advanced pH Measurement and Control, 3rd Ed. Gregory K. McMillan
      46. Analysis of Cosmetic Products. Amparo Salvador 2007
      47. Analysis of Drug Impurities (Sheffield Analytical Chemistry Series). Richard J. Smith 2007
      48. Analytical method Validation and Instrument Performance Verification. Chung Chow Chan 2004
      49. Calibration in the Pharmaceutical Laboratory. Tony Kowalski 2001.
      50. Chromatographic Integration Methods (Rsc Chromatography Monographs). N. Dyson 1998
      51. Chromatography of Antibiotics (Journal of Chromatography Library). Gerald H. Wagman 1973
      52. Chromatography of Antibiotics, 2nd Ed ( Journal of Chromatography Library). Gerald H. Wagman 1984
      53. Clarkes Analysis of Drugs and Poisons, 3rd Ed. Laurent Y Galichet 2005
      54. Clarkes Isolation and Identification of Drugs, 2nd Ed 1986
      55. Columns for Gas Chromatography: Performance and Selection. Eugene F. Barry 2007
      56. Development and Validation of Analytical Methods (Progress in Pharmaceutical and Biomedical Analysis). C.M. Riley 1996
      57. Handbook of Analytical Techniques (2 Vol Set). Helmut Günzler 2001
      58. Handbook of Basic Tables for Chemical Analysis, Second Edition. Thomas J. Bruno 2003
      59. Handbook of Media for Environmental Microbiology, 2nd Ed. Ronald M Atlas 2005
      60. Handbook of Microbiological Media for the Examination of Food, 2nd Ed. Ronald M Atlas 2006
      61. Handbook of Microbiological Media, 3rd Ed. Ronald M Atlas 2004
      62. Handbook of Modern Pharmaceutical Analysis (Separation Science and Technology). Satinder Ahuja 2001
      63. Handbook of Organic Compounds (3 Vol Set): NIR, IR, Raman, and UV-Vis Spectra Featuring Polymers and Surfactants. Jr., Jerry Workman 2000
      64. Handbook of Pharmaceutical Analysis (Drugs and the Pharmaceutical Sciences). Lena Ohannesian 2002
      65. Handbook of Pharmaceutical Analysis by HPLC. Satinder Ahuja 2005.
      66. Handbook of Process Chromatography, 2nd Edition: Development, Manufacturing, Validation and Economics. Lars Hagel 2007
      67. Handbook of Stability Testing in Pharmaceutical Development: Regulations, Methodologies, and Best Practices. Kim Huynh-Ba 2008
      68. Handbook of Thin Layer Chromatography, 3rd Ed. Joseph Serma 2003
      69. Handbook of Vibrational Spectroscopy (5 Vol set). John M. Chalmers 2002
      70. High-Throughput Analysis in the Pharmaceutical Industry. Perry G. Wang 2009.
      71. HPLC Made to Measure: A Practical Handbook for Optimization. Stavros Kromidas 2006
      72. Identification and Determination of Impurities in Drugs (Progress in Pharmaceutical and Biomedical Analysis - Volume 4). S. Görög 2000
      73. Illustrated Pocket Dictionary of Chromatography. Paul C. Sadek 2004.
      74. Impurities Evaluation of Pharmaceuticals. Satinder Ahuja 1998
      75. Lange`s Handbook of Chemistry, 16th Ed. James G. Speight 2005
      76. Method Validation in Pharmaceutical Analysis. J. Ermer 2005
      77. More Practical Problem Solving in HPLC. Stavros Kromidas 2004
      78. Particle Size Analysis (Special Publications). N. G. Stanley-Wood 1992
      79. Particle Size Analysis In Pharmaceutics And Other Industries, Theory And Practice. Washington, 1992.
      80. Pharmaceutical Analysis (Sheffield Analytical Chemistry Series). David C. Lee 2003
      81. Pharmaceutical Analysis-A textbook for pharm student and pharm chemist. David G Watson 1999
      82. Pharmaceutical Chemical Analysis:Methods for Identification and Limit Tests. Ole Pedersen 2006.
      83. Pharmaceutical Dissolution Testing. Jennifer Dressman 2005
      84. Pharmaceutical Drug Analysis. Ashutosh Kar 2005
      85. Pharmaceutical Stress Testing. Steven W. Baertschi 2005
      86. Powder Sampling and Particle Size Determination. Terrence Allen 2004
      87. Practical Problem Solving in HPLC. Stavros Kromidas 2000
      88. Rapid Microbiological Methods in the Pharmaceutical Industry. Martin C.Easter 2005
      89. Reference Materials for Chemical Analysis: Certification, Availability, and Proper Usage. Markus Stoeppler 2001
      90. Robustness of Analytical Chemical Methods and Pharmaceutical Technological Products. Margriet M.W.B. Hendriks 1996
      91. Sampling and Sample Preparation for Field and Laboratory. Janusz Pawliszyn
      92. Solving Problems with NMR Spectroscopy. Atta-ur-Rahman 1995
      93. Spectroscopy of Pharmaceutical Solids (Drugs and the Pharmaceutical Sciences). Harry G. Brittain 2006
      94. Statistical Design and Analysis of Stability Studies. Shein-Chung Chow 2007
      95. The Troubleshooting and Maintenance Guide for Gas Chromatographers, 4th Ed. Dean Rood 2007
      96. Thermal Analysis of Pharmaceuticals. Duncan Q.M. Craig 2007
      97. Trace Quantitative Analysis By Mass Spectrometry. Robert K. Boyd 2008
      98. Troubleshooting LC Systems: A Comprehensive Approach to Troubleshooting LC Equipment and Separations. John W. Dolan 1989
      99. Validation and Qualification in Analytical Laboratories, Second Edition. Ludwig Huber 2007
      100. Validation of Chromatography Data Systems (Rsc Chromatography Monographs). R D McDowall 2005
DUA
      1. British Pharmacopoeia 2009
      2. European Pharmacopoeia, 5th Ed. Main Volume 5.0, 2005
      3. Japanese Pharmacopeia, 15th Ed (Pharmacopoeia of Japan). Yakuji Nippo Ltd 2006
      4. The International Pharmacopoeia, Vol. 5 (Third Edition). World Health Organization 2003
      5. USP NF 2009 (United States Pharmacopeia 32 / National Formulary 27)
      6. ISO 14001 Environmental Certification Step by Step: Revised Edition. A.J. Edwards 2004
      7. ISO 14001 Environmental Systems Handbook, Second Edition. Ken Whitelaw 2004
      8. ISO 9000 Quality Systems Handbook, 4th Ed. David Hoyle 2001
      9. ISO 9000 Quality Systems Handbook, 5th Ed. David Hoyle 2006
      10. ISO 9001: 2000 in Brief. Ray Tricker 2001
      11. ISO 9001:2000 Quality Management System Design. Jay Schlickman 2003
      12. GLP Quality Audit Manual, 3rd Edition. Milton A. Anderson 2002
      13. GMP/ISO Quality Audit Manual for Healthcare Manufacturers and their Suppliers, Sixth Edition, (Volume 1 - With Checklis). Leonard Steinborn 2003
      14. GMP/ISO Quality Audit Manual for Healthcare Manufacturers and Their Suppliers, Sixth Edition, (Volume 2 - Regulations, Standards, and Guidelines). Leonard Steinborn 2005
      15. Good Clinical, Laboratory and Manufacturing Practices: Techniques for the QA Professional. P. Carson 2007
      16. Good Design Practices for GMP Pharmaceutical Facilities. Andrew A. Signore 2005
      17. Good Laboratory Practice Regulations, 3rd Ed. Revised and Expanded. Sandy Weinberg 2003
      18. Good Laboratory Practice Regulations, 4th Ed. Sandy Weinberg 2007
      19. Good Laboratory Practice: OECD Principles And Guidance for Compliance Monitoring. Organisation for Economic Co-operation and Development 2005
      20. Good Laboratory Practice: the Why and the How, 2nd Ed. Jürg P. Seiler 2005
      21. Good Manufacturing Practices for Pharmaceutical: A Plan for Total Quality Control From Manufacturer to Consumer, 5th Ed. Sidney H. Wig 2001
      22. Good Manufacturing Practices for Pharmaceuticals, Sixth Edition. Joseph D. Nally 2007
      23. Good Pharmaceutical Manufacturing Practice : Rationale and Compliance. John Sharp 2005
      24. Pharmaceutical and Medical Device Validation By Experimental Design. Lynn D. Torbeck 2007
      25. Pharmaceutical Engineering Change Control, 2nd Ed. Simon G. Turner 2004.
      26. Pharmaceutical Innovation: Incentives, Competition, and Cost-Benefit Analysis in International Perspective. Frank A sloan 2007
      27. Pharmaceutical Manufacturing Handbook: Regulations and Quality (Pharmaceutical Development Series). Shayne Cox Gad 2008
      28. Pharmaceutical Marketing - A Practical Guide. Dimitris Dogramatzis 2002.
      29. Pharmaceutical Master Validation Plan - The Ultimate Guide to FDA, GMP, and GLP Compliance. Syed Imtiaz Haider, 2002.
      30. Pharmaceutical Pre-Approval Inspections: A Guide to Regulatory Success, Second Edition (Drugs and the Pharmaceutical Sciences). Martin D. Hynes III 2008
      31. Pharmaceutical Process Validation: An International Third Edition (Drugs and the Pharmaceutical Sciences). Robert A. Nash 2003
      32. Pharmaceutical Product Branding Strategies: Simulating Patient Flow and Portfolio Dynamics, Second Edition. Corey Peck 2009
      33. Pharmaceutical Product Strategy: Using Dynamic Modeling for Effective Brand Planning. Mark Paich 2005
      34. Pharmaceutical Project Management (Drugs and the Pharmaceutical Sciences, Volume 86). Tony Kennedy 1998
      35. Pharmaceutical Project Management, 2nd edition (Drugs and the Pharmaceutical Sciences). Tony Kennedy 2008
      36. Quality (Pharmaceutical Engineering Series), Volume 2 . Kate McCormick 2002
      37. Quality Assurance in Analytical Chemistry (Analytical Techniques in the Sciences). Elizabeth Prichard 2007
      38. Quality Assurance in Analytical Chemistry, 2nd Ed. Werner Funk 2007
      39. Quality Assurance in Environmental Monitoring: Sampling and Sample Pretreatment. Ph Quevauviller 1995
      40. Quality Assurance in the Analytical Chemistry Laboratory. D. Brynn Hibbert 2007
      41. Quality assurance of pharmaceuticals: A compendium of guidelines and related materials. Vol 2, Updated edition. WHO 2004
      42. Quality Assurance of Pharmaceuticals: A compendium of guidelines and related materials-Vol 2, 2nd updated edition . WHO 2007
      43. Quality Engineering Handbook, Second Edition, Revised and Expanded (Quality and Reliability). Thomas Pyzdek 2003
      44. Quality Management System Handbook for Product Development Companies. Vivek Nanda 2005
      45. Quality Systems and Controls for Pharmaceuticals. Dipak Kumar Sarker 2008
      46. 21 CFR Part 11 - Complete Guide to International Computer Validation Compliance for the Pharmaceutical Industry. Orlando López 2004.
      47. A Primer on Quality in the Analytical Laboratory. John Kenkel 2000
      48. Automation and Validation of Information in Pharmaceutical Processing (Drugs & the Pharmaceutical Sciences). Despautz 1998
      49. Batch Control Systems: Design, Application, and Implementation, 2nd Ed. William M. Hawkins 2006
      50. Batch Processes. Ekaterini Korovessi 2006
      51. Business Development for the Biotechnology and Pharmaceutical Industry. Martin Austin 2008
      52. Combination Products: Regulatory Challenges and Successful Product Development. Smita Gopalaswamy 2008
      53. Compact Regs Parts 210 and 211: CFR 21 Parts 210 and 211 Pharmaceutical and Bulk Chemical GMPs (10 Pack).Food and Drug Administration 2005
      54. Compliance Handbook for Pharmaceuticals, Medical Devices, and Biologics. Carmen Medina 2004
      55. Computer System Validation. Guy Wingate 2004
      56. Establishing A CGMP Laboratory Audit System: A Practical Guide. David M. Bliesner 2006
      57. Facility Validation: Theory, Practice,and Tools. Graham C. Wrigley 2004
      58. Forecasting for the Pharmaceutical Industry: Models for New Product And In-market Forecasting And How to Use Them. Arthur G. Cook 2006
      59. Get Set & Grow:A Handbook For Medical Representative, 3rd Ed. Vivek Mehrotra 2007
      60. Global Pharmaceutical Marketing - A practical guide to codes and compliance. Judith Grice 2008.
      61. Guidance for the Implementation of a Quality Management System in Drug Testing Laboratories: A Commitment to Quality and Continuous Improvement. United Nations 2009
      62. Guidelines for Auditing Process Safety Management Systems. Center for Chemical Process Safety (CCPS) 1993
      63. Guidelines for Chemical Transportation Safety, Security, and Risk Management. Center for Chemical Process Safety (CCPS) 2008
      64. Guidelines for Implementing Process Safety Management Systems. Center for Chemical Process Safety (CCPS) 1994
      65. Guidelines for Investigating Chemical Process Incidents, 2nd Edition. American Institute of Chemical Engineers 2003
      66. Guidelines for Process Hazards Analysis (PHA, HAZOP), Hazards Identification, and Risk Analysis. Nigel Hyatt 2003
      67. Guidelines for Safe Handling of Powders and Bulk Solids. Center for Chemical Process Safety (CCPS) 2005
      68. Guidelines for the Import and Export of Drug and Precursor Reference Standards for use by National Drug Testing Laboratories and Competent National Authorities. United Nations 2007
      69. Guidelines for The Safe Handling and Disposal of Chemicals Used in the Illicit Manufacturing of Drugs. United Nations Office on Drugs and Crime 2006
      70. Handbook of Production Scheduling (International Series in Operations Research & Management Science). Jeffrey W. Herrmann 2006
      71. Instrumentation and Control Systems Documentation. Frederick A. Meier 2004
      72. Integrating ISO 14001 into A Quality Management System, 2nd Ed. Marilyn R. Block 2002
      73. International IT Regulations and Compliance: Quality Standards in the Pharmaceutical and Regulated Industries. Siri H. Segalstad 2008
      74. International Pharmaceutical Registration. Alan A. Chalmers 2000
      75. Inventory Control and Management, 2nd Edition. Donald Waters 2003
      76. Laboratory Auditing For Quality and Regulatory Compliance. Donald C. Singer 2005.
      77. Leading Pharmaceutical Innovation: Trends and Drivers for Growth in the Pharmaceutical Industry, 2nd Ed. Oliver Gassmann 2008
      78. Operations Management. S. Anil Kumar 2009
      79. Principles and Practices of Method Validation (Proceedings of the Joint AOAC/FAO/IAEA/ILJPAC International Workshop). A. Fajgelj 2000
      80. Production and Operations Management, 2nd Ed. S. Anil Kumar 2008
      81. Research and Development Management in the Chemical and Pharmaceutical Industry. Peter Bamfield 2003
      82. Risk-sharing in the Pharmaceutical Industry: The Case of Out-licensing (Contributions to Management Science). Gerrit Reepmeyer 2006
      83. Rules and Guidance for Pharmaceutical Manufacturers and Distributors. MHRA 2007
      84. Six SIGMA for Quality and Productivity Promotion (Productivity Series 32). Sung H. Park 2003
      85. Six Sigma in the Pharmaceutical Industry: Understanding, Reducing, and Controlling Variation in Pharmaceuticals and Biologics. Brian K. Nunnally 2007
      86. The Laboratory Quality Assurance System, 3rd Ed: A Manual of Quality Procedures and Forms. Thomas A. Ratliff 2003
      87. The Management of Chemical Process Development in the Pharmaceutical Industry. Derek Walker 2008
      88. The Pharmaceutical Regulatory Process, 2nd Ed. Ira R. Berry 2008
      89. The Pharmaceutical Regulatory Process. Ira R. Berry 2005
      90. Total R & D Management: Strategies and Tactics for 21st Century Healthcare Manufacturers. Roger Dabbah 1999
      91. Validating Corporate Computer Systems: Good IT Practice for Pharmaceutical Manufacturers. Guy Wingate 2000
      92. Validating Medical Packaging. Ronald Pilchik 2003
      93. Validating Pharmaceutical Systems: Good Computer Practice in Life Science Manufacturing. John Andrews 2005
      94. Validation in Chemical Measurement. Paul De Bièvre 2005
      95. Validation of Pharmaceutical Processes, 3rd Ed. James P. Agalloco 2008
      96. Validation Standard Operating Procedures: A Step by Step Guide for Achieving Compliance in the Pharmaceutical, Medical Device, and Biotech Industries, 2nd Ed. Syed Imtiaz Haider 2006
      97. Validation Standard Operating Procedures: A Step by Step Guide for Achieving Compliance in the Pharmaceutical, Medical Device, and Biotech Industries. Syed Imtiaz Haider 2002
      98. Warehouse Management: Automation and Organisation of Warehouse and Order Picking Systems . Michael ten Hompel 2007
      99. Who Expert Committee on Specifications for Pharmaceutical Preparations (Technical Report Series). WHO 2008
      100. Write It Down: Guidance for Preparing Effective and Compliant Documentation, 2nd Ed. Janet Gough 2005
TIGA

 

      1. Handbook The Merck Index, 13th Ed -An Encyclopedia Of Chemicals, Drugs, And Biological
      2. Handbook for Critical Cleaning: Aqueous, Solvent, Advanced Processes,Surface Preparation, and Contamination Control. Barbara Kanegsberg 2001
      3. Handbook of Aqueous Solubility Data. Samuel H. Yalkowsky 2003
      4. Handbook of Industrial Mixing: Science and Practice. Edward L. Paul 2004
      5. Handbook of Ozone Technology and Applications. Aharon Netzer 1985
      6. Handbook of Pharm Manufacturing Formulations-Liquid Products. Sarfaraz K. Niazi 2004
      7. Handbook of Pharm Manufacturing Formulations-OTC Products. Sarfaraz K. Niazi 2004
      8. Handbook of Pharm Manufacturing Formulations-Sterile Products. Sarfaraz K. Niazi 2004
      9. Handbook of Preformulation: Chemical, Biological, and Botanical Drugs. Sarfaraz K. Niazi 2007
      10. Handbook of Water and Wastewater Treatment Technologies, First Edition. Nicholas P. Cheremisinoff 2002
      11. Handbook of Water Treatment, 2nd English Edition. KURITA WATER INDUSTRIES LTD 1999
      12. Pharmaceutical Dosage Forms: Disperse systems, Vol 1. Herbert Lieberman 1996
      13. Pharmaceutical Dosage Forms: Disperse Systems, Vol 2. Herbert Lieberman 1996
      14. Pharmaceutical Dosage Forms: Disperse Systems, Vol 3. Herbert Lieberman 1998
      15. Pharmaceutical Dosage Forms: Parenteral Medications, Volume 1. Kenneth E. Avis 1993
      16. Pharmaceutical Dosage Forms: Parenteral Medications, Volume 2. Kenneth E. Avis 1993
      17. Pharmaceutical Dosage Forms: Parenteral Medications, Volume 3. Kenneth E. Avis 1993
      18. Pharmaceutical Emulsions and Suspensions. Francoise Nielloud 2000
      19. Pharmaceutical Experimental Design and Interpretation, 2nd Ed. N. Anthony Armstrong 2006
      20. Pharmaceutical Extrusion Technology. Isaac Ghebre-Sellassie 2003.
      21. Pharmaceutical Formulation Development of Peptides and Proteins . Sven Frokjaer 2000
      22. Pharmaceutical Inhalation Aerosol Technology, 2nd Ed. Revised and Expanded. Anthony J. Hickey 2004
      23. Pharmaceutical Manufacturing Encyclopedia, 2nd Ed, Vol 1. Marshall Sittig 1988.
      24. Pharmaceutical Manufacturing Encyclopedia, 3rd Ed . William Andrew Publishing 2007
      25. Pharmaceutical Manufacturing Handbook: Production and Processes (Pharmaceutical Development Series). Shayne Cox Gad 2008
      26. Pharmaceutical Packaging Technology. D.A.Dean 2000
      27. Pharmaceutical Preformulation and Formulation - A Practical Guide from Candidate Drug Selection to Commercial Dosage Form. Mark Gibson 2004.
      28. Pharmaceutical Process Engineering. Anthony J Hickey 2001
      29. Pharmaceutical Production - An Enginering Guide. Bill Bennet 2003.
      30. Pharmaceutical Production Facilities: Design and Applications, 2nd Ed . Graham Cole 1998
      31. Pharmaceutical Substances, 4th Ed. Axel Kleemann 2000
      32. A Comprehensive Guide to the Hazardous Properties of Chemical Substances, 3rd Ed. Pradyot Patnaik 2007
      33. Achieving Sterility Medical and Pharmaceutical Products. Nigel A. Hals 1994
      34. Active Pharmaceutical Ingredients:Development, Manufacturing, and Regulation.Stanley H. Nusim 2005
      35. Aerosol Measurement: Principles, Techniques, and Applications, 2nd Ed. Paul A. Baron 2001
      36. Aerosol Science: Theory and Practice. M. M. R. Williams 1991
      37. Alternative sweeteners, 3rd Ed. Lyn O’Brien Nabors 2001.
      38. Chemical Compounds ( 3 Vol Set). Neil Schlager 2006
      39. Clean-In-Place for Biopharmaceutical Processes. Dale A. Seiberling 2008.
      40. Cleanroom Technology: Fundamentals of Design, Testing and Operation. W White 2001
      41. Contamination And Esd Control In High-Technology Manufacturing. Roger W.Welker 2006
      42. Control Systems for Heating, Ventilating, and Air Conditioning, 6th Ed. Roger W. Haines 2006
      43. Development of Biopharmaceutical Parenteral Dosage Forms (Drugs and the Pharmaceutical Sciences). John A. Bontempo 1997
      44. Drug Delivery to the Lung (Lung Biology in Health and Disease). Hans Bisgaard 2002
      45. Drug Products for Clinical Trials, 2nd Ed. Monkhouse 2006.
      46. Emulsifying Agents: An Industrial Guide. Ernest W. Flick 1990
      47. Endotoxins: Pyrogens, LAL Testing and Depyrogenation, 3rd Ed (Drugs and The Pharmaceutical Sciences). Kevin L. Williams 2007
      48. Environmental Monitoring for Cleanrooms and Controlled Environments. Anne Marie Dixon 2007
      49. Excipient Development for Pharmaceutical, Biotechnology, and Drug Delivery Systems. Ashok Katdare 2006
      50. FASTtrack: Pharmaceutics - Dosage Form and Design. David Jones 2008
      51. Fenner's Complete Formulary and Handbook, 6th Ed. B Fenner 1988
      52. Filters and Filtration Handbook, 5th Ed. Ken Sutherland 2008
      53. Filtration and Purification in the Biopharmaceutical Industry, 2nd Edition (Drugs and the Pharmaceutical Sciences). Maik W. Jornitz 2007
      54. Fluid Sterilization by Filtration, Third Edition. Peter R. Johnston 2004
      55. Food Chemical Codex, 5th Ed. 2004.
      56. Groundwater Chemicals Desk Reference, Fourth Edition. John H. Montgomery 2007
      57. Hansen Solubility Parameters: A User's Handbook, Second Edition. Charles M. Hansen 2007
      58. HVAC Equations, Data and Rules of Thumb, 2nd Ed. Arthur A. Bell Jr 2007
      59. HVAC Fundamentals, 2nd Ed. Samuel C. Sugarman 2007
      60. Industrial Solvents Handbook. Archer 1996
      61. Inhalation, Studies Foundations and Techniques, 2nd Ed. Robert F. Phalen 2009
      62. Injectable Dispersed Systems: Formulation, Processing, and Performance. Diane J. Burgess 2005.
      63. Intraocular Drug Delivery. Glenn J. Jaffe 2006
      64. Microbial Contamination Control in Parenteral Manufacturing. Kevin L.Williams 2004.
      65. Microbial Contamination Control in the Pharmaceutical Industry (Drugs and the Pharmaceutical Sciences). Luis Jimenez 2004
      66. Microbial Limit and Bioburden Tests: Validation Approaches and Global Requirements,Second Edition. Lucia Clontz 2009
      67. Microbiological Contamination Control in Pharmaceutical Clean Rooms. Nigel Halls 2004.
      68. Modern Pharmaceutics, 4th Ed Revised and Expanded. Gilbert S. Banker 2002
      69. Modern Pharmaceutics, 5th Ed, Vol 2: Applications and Advances (Drugs and the Pharmaceutical Sciences). Alexander T. Florence 2009
      70. NIOSH Pocket Guide to Chemical Hazards
      71. Ocular Transporters in Ophthalmic Diseases and Drug Delivery (Ophthalmology Research). Joyce Tombran-Tink 2008
      72. Ophthalmic Drug Delivery Systems, 2nd Ed.Revised and Expanded. Ashim K. Mitra 2003
      73. Oral Lipid-Based Formulations: Enhancing the Bioavailability of Poorly Water-Soluble Drugs. David J. Hauss 2007
      74. Over the Counter Pharmaceutical Formulations. David D. Braun 1994
      75. Packaging Closures and Sealing Systems (Sheffield Packaging Technology). Nigel Theobald 2006
      76. Parenteral Quality Control: Sterility, Pyrogen, Particulate,and Package Integrity Testing, 2nd Ed. Michael J. Akers 1994
      77. Parenteral Quality Control: Sterility, Pyrogen, Particulate,and Package Integrity Testing, 3rd Ed. Michael J. Akers 2003.
      78. Particulate Interactions in Dry Powder Formulations for Inhalation. Xian Ming Zeng 2001
      79. Pharmaceutical Applications of Polymers for Drug Delivery (Rapra Review Reports). D. Jones 2004
      80. Pharmaceutics: The Science of Dosage Form Design, 2nd Ed. M.E Aulton
      81. Physical-Chemical Treatment of Water and Wastewater. Arcadio P. Sincero 2003
      82. Physicochemical Principles of Pharmacy, 4th Ed. Alexander T Florence 2006
      83. Plastic Packaging: Interactions with Food and Pharmaceuticals. Otto G. Piringer 2008
      84. Preliminary Studies to Determine the Shelf Life of HEPA Filters. H. Gilbert Present at 23rd DOE/NRC Nuclear Air Cleaning and Treatment Conference Buffalo, NY July 24-28, 1994
      85. Role of Lipid Excipients in Modifying Oral and Parenteral Drug Delivery: Basic Principles and Biological Examples. Kishor M. Wasan 2007
      86. Sterile Filtration: A Practical Approach.Maik W. Jornitz 2001
      87. Sterile Product Facility Design and Project Management, 2nd Ed. Jeffery N. Odum 2004.
      88. Sterilisation of Polymer Healthcare Products. Wayne Rogers 2005
      89. Sterilization Validation and Routine Operation Handbook: Radiation. Anne F. Booth 2001
      90. Supercritical Fluid Technology for Drug Product Development (Drugs and the Pharmaceutical Sciences). Peter York 2004
      91. Surfactants and Polymers in Drug Delivery. Martin Malmsten 2002
      92. The 100 Most Important Chemical Compounds: A Reference Guide. Richard L. Myers 2007
      93. The Aqueous Cleaning Handbook: A Guide to Critical-Cleaning Procedures, Techniques and Validation, 3rd Ed. Malcolm C. McLaughlin 2002
      94. The Effects of Sterilization Methods on Plastics and Elastomers, 2nd Ed: The Definitive User’s Guide and Databook. Liesl K. Massey 2005
      95. The Mechanics of Inhaled Pharmaceutical Aerosols. Warren H. Finlay 2001.
      96. Ultraviolet Light in Water and Wastewater Sanitation. Willy J. Masschelein 2002
      97. Validated Cleaning Technologies for Pharmaceutical Manufacturing. Destin A. LeBlanc 2000
      98. Water-Insoluble Drug Formulation, Second Edition. Rong Liu 2008
      99. Wiley Guide to Chemical Incompatibilities, 2nd Ed. Richard P. Pohanish 2003
      100. Wiley’s Remediation Technologies Handbook: Major Contaminant Chemicals and Chemical Groups. Jay H Lehr 2004
EMPAT
      1. Handbook of Pharmaceutical Excipients, 6th Edition. Raymond C. Rowe 2009
      2. Encyclopedia of Pharmaceutical Technology, 3rd Ed (6 Vol Set). James Swarbrick 2007
      3. Encyclopedia of Pharmaceutical Technology, Vol 20. James Swarbrick 2001
      4. Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals, 2nd Ed, Vol 1: Introduction and Hydrocarbons. Donald McKay 2006
      5. Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals, 2nd Ed, Vol 2: Halogenated Hydrocarbons. Donald McKay 2006
      6. Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals, 2nd Ed, Vol 3: Oxygen Containing Compounds. Donald McKay 2006
      7. Handbook of Physical-Chemical Properties and Environmental Fate for Organic Chemicals, 2nd Ed, Vol 4: Nitrogen and Sulfur Containing Compounds and Pesticides. Donald McKay 2006
      8. The Dictionary of Substances and their effects, 2nd Ed, Vol 1. Royal Society of Chemistry 1999
      9. The Dictionary of Substances and their effects, 2nd Ed, Vol 2. Royal Society of Chemistry 1999
      10. The Dictionary of Substances and their effects, 2nd Ed, Vol 3. Royal Society of Chemistry 1999
      11. The Dictionary of Substances and their effects, 2nd Ed, Vol 4. Royal Society of Chemistry 1999
      12. The Dictionary of Substances and their effects, 2nd Ed, Vol 5. Royal Society of Chemistry 1999
      13. The Dictionary of Substances and their effects, 2nd Ed, Vol 6. Royal Society of Chemistry 1999
      14. The Dictionary of Substances and their effects, 2nd Ed, Vol 7. Royal Society of Chemistry 1999
      15. Handbook of Conveying and Handling of Particulate Solids, Volume 10 (Handbook of Powder Technology). A. Levy, H. Kalman 2001
      16. Handbook of Cosmetic Science and Technology, 2nd Ed. Marc Paye 2006
      17. Handbook of Cosmetic Science and Technology, 3rd Ed. Andre O. Barel 2009
      18. Handbook of Cosmetic Science and Technology, André O. Barel 2001
      19. Handbook of Pharm Manufacturing Formulations-Uncompressed Solid Products. Sarfaraz K. Niazi 2004
      20. Handbook of Pharmaceutical Controlled Release Technology. Donald L. Wise 2000
      21. Handbook of Pharmaceutical Granulation Technology, Second Edition. Dilip M. Parikh 2005
      22. Handbook of Porous Solids (4 Vol Set). Ferdi Schüth 2002
      23. Handbook of Pharm Manufacturing Formulations-Compressed Solid Products. Sarfaraz K. Niazi 2004
      24. Handbook of Pharm Manufacturing Formulations- Semisolid Products. Sarfaraz K. Niazi 2004
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      28. Cosmetic and Toiletry Formulation, 2nd Ed-Vol 4. Ernest w. Flick 1996
      29. Cosmetic and Toiletry Formulation, 2nd Ed-Vol 5. Ernest w. Flick 1996
      30. Cosmetic and Toiletry Formulation, 2nd Ed-Vol 6. Ernest w. Flick 1997
      31. Cosmetic and Toiletry Formulation, 2nd Ed-Vol 7. Ernest w. Flick 1999
      32. Cosmetic and Toiletry Formulation, 2nd Ed-Vol 8. Ernest w. Flick 2001
      33. A Practical Approach to Rheology and Rheometry. Gebhard Schramm 1994
      34. Advanced Drying Technologies, Second Edition. Tadeusz Kudra 2009
      35. Advanced Pharmaceutical Solids (Drugs and the Pharmaceutical Sciences). Jens T. Carstensen 2001
      36. Advances in Pharmaceutical Sciences. David Ganderton 1995
      37. Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms, 3rd Ed (Drugs and the Pharmaceutical Sciences). James W. McGinity 2008
      38. Bulk Solids Handling: Equipment Selection and Operation,1st Ed. Don McGlinchey 2008
      39. Coatings Technology Handbook, Third Edition. Arthur A. Tracton. Arthur A. Tracton 2006
      40. Coatings Technology: Fundamentals, Testing, and Processing Techniques. Arthur A. Tracton 2007
      41. Computational Plasticity in Powder Forming Processes. Amir R. Khoei 2005.
      42. Conditioning Agents for Hair and Skin (Cosmetic Science and Technology Series). Randy Schueller 1999
      43. Cosmetic Formulation of Skin Care Products. Zoe Diana Draelos 2006.
      44. Cosmetic Microbiology: A Practical Approach, 2nd Ed. Philip A. Geis 2006
      45. Cosmetics Additives: An Industrial Guide. Ernest W. Flick 1991
      46. Delivery System Handbook for Personal Care and Cosmetic Products: Technology, Applications, and Formulations. Meyer R. Rosen 2005
      47. Dermatologic, Cosmeceutic, and Cosmetic Development: Therapeutic and Novel Approaches. Kenneth A. Walters 2008
      48. Dermatological and Transdermal Formulations. Kenneth A. Walters 2002
      49. Design of Controlled Release Drug Delivery Systems. Xiaoling Li 2006
      50. Developing Solid Oral Dosage Forms: Pharmaceutical Theory & Practice. Yihong Qiu 2009
      51. Drug Delivery Systems (Methods in Molecular Biology). Kewal K. Jain 2008
      52. Drug Delivery Systems, 2nd Ed. Vasant V. Ranade 2004
      53. Drug Delivery to the Oral Cavity: Molecules to Market. Tapash K. Ghosh 2005
      54. Drug Permeation Enhancement: Theory and Applications (Drugs and the Pharmaceutical Sciences). Dean S. Hsieh 1994
      55. Drug Photochemistry and Photostability. A. Albini 1998
      56. Drug Stability:Principles and Practice, 3rd Ed. Jens T Cartenssen 2000
      57. Drying of Porous Materials. Stefan Jan Kowalski 2007
      58. Encyclopedia of Controlled Drug Delivery (2 Vol Set). Edith Mathiowitz 1999
      59. Enhancement in Drug Delivery. Elka Touitou 2007
      60. Formulation and Analytical Development for Low-Dose Oral Drug Products. Jack Zheng 2009
      61. Formulation Technology: Emulsions, Suspensions, Solid Forms. Hans Mollet 2001
      62. Freeze-Drying, Second Edition. Georg-Wilhelm Oetjen 2004
      63. Freeze-Drying/lyophilization of Pharmaceutical and Biological Products, 2nd Ed Revised and Expanded. Louis Rey 2004
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LIMA
  1. Handbook of Pharmaceutical Excipients, 5th Edition. Raymond C. Rowe 2006
  2. Powder and Bulk Engineering International July 2009
  3. Powder and Bulk Engineering International Magazine January 2009
  4. Powder and Bulk Engineering International Sep/Oct-2008
  5. Powder and Bulk Engineering International, May 2009
  1. The Merck Index 12th ed.
  2. CleanRooms - Magazines Februari 2008
  3. CleanRooms - Magazines Januari 2008
  4. Controlled Environment - July / Aug 2008. Vicon Publishing, Inc
  5. Controlled Environments - November 2008
  6. Controlled Environments May 2008
  1. British Pharmacopoeia 2007
  2. USP NF 2007 (United States Pharmacopeia 30 / National Formulary 25)
  3. Perundangan Kesehatan dan Keselamatan Kerja (K3) - ISO 17025
  4. CleanRooms - Magazines Maret 2008
  5. CleanRooms - Magazines April 2008
  6. CleanRooms - Magazines Mei 2008
  1. Chemical Engineering Magazine - April 2009
  2. Pharmaceutical Engineering - July/August 2008
  3. Pharmaceutical Engineering - May/June 2008
  4. Pharmaceutical Engineering Magazine Jan/Feb 2009

Sumber www.ebookfarmasi.tk

9 comments:

Irwan Setiawan Kilay said...

salam kenal.nama saya irwan.

Saya sedang belajar tentang farmasi fasility.
Boleh share buku "Pharmaceutical Production Facilities: Design and Applications, 2nd Ed . Graham Cole 1998" ? karena website www.ebookfarmasi.tk sudah ga bisa diakses lagi.

kalo ada, minta tolong send ke email saya irwan.kilay@gmail.com.

terima kasih,

irwan

andy wibowo said...

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sandra said...

sayaingin download beberapa buku bagaimana caranya? sudah coba buka linknya tapi telah dihapus....

andy wibowo said...

buku apa saja mas,/?kirim kan email, nanti saya usahakan carikan....karena saya sekarang, di blog ini lagi ada program
http://itheng.blogspot.com/2012/09/1000-literatur-farmasi-untuk-mahasiswa.html

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Leo Kurniawan said...

Kepada yth Pengelolah Blog ini,

Boleh minta informasi tentang cara dan juga rregulasi untuk import bahan excipient untuk keperluan farmasi di Indonesia ?

Bila ada mohon bisa dikirim ke lamat email saya

leokurniawandr@gmail.com
Terima kasih banyak sebelumnya,

Salam,

Dr. Leo Kurniawan
www.selukbelukkvaksin.com

Anonymous said...

mas ... saya mau ebooknya ... mint tolong juga send ke email saya ya mas di galihau@gmail.com :)
mkasih sebelumnya .....