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Daftar E-Book DVD Kompilasi Industri 1

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 Gnzler 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. Grg 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
Bonus :

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
Daftar E-book DVD Kompilasi Industri 2

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, Andr 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 Schth 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
25. Cosmetic and Toiletry Formulation, 2nd Ed-Vol 1. Ernest w. Flick 1989
26. Cosmetic and Toiletry Formulation, 2nd Ed-Vol 2. Ernest w. Flick 1992
27. Cosmetic and Toiletry Formulation, 2nd Ed-Vol 3. Ernest w. Flick 1995
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
64. Generic Drug Development: Solid Oral Dosage Forms. Leon Shargel 2005
65. Generic Drug Formulations. Volker Bhler 1998
66. Granulation (Handbook of Powder Technology, Volume 11). Agba D. Salman 2006
67. Isolation Technology: A Practical Guide, Second Edition. Tim Coles 2004
68. Mechanisms of Transdermal Drug Delivery. Russell. 0. Potts 1997
69. Microencapsulation (Drugs and the Pharmaceutical Sciences). Simon Benita 1996
70. Microencapsulation: Methods and Industrial Applications, 2nd Ed (Drugs and the Pharmaceutical
Sciences). Simon Benita 2006
71. Modified-Release Drug Delivery Technology. Michael J. Rathbone 2003
72. Novel Cosmetic Delivery Systems (Cosmetic Science and Technology , Vol 19). Elka Touitou 1999
73. Oral Delivery of Macromolecular Drugs: Barriers, Strategies and Future Trends. Andreas Bernkop-
Schnrch 2009
74. Particle Breakage (Handbook of Powder Technology, Volume 12). Agba D. Salman 2007
75. Percutaneous Absorption: Drugs, Cosmetics, Mechanisms, Methods, Fourth Edition (Drugs and the
Pharmaceutical Sciences). Robert L. Bronaugh 2005
76. Percutaneous Absorption: Drugs--Cosmetics--Mechanisms--Methodology, Third Edition, (Drugs and the
Pharmaceutical Sciences, V. 97,). Robert L. Bronaugh 1999
77. Percutaneous Penetration Enhancers, 2nd Ed. Eric W. Smith 2006
78. Pharmaceutical Coating Technology (Pharmaceutical Sciences Series). Graham Cole 1995
79. Pharmaceutical Dosage Forms: Tablets, Volume 1, 2nd Ed. Herbert A.Lieberman 1989
80. Pharmaceutical Dosage Forms: Tablets, Volume 1, 3rd Ed : Unit Operations and Mechanical Properties.
Larry L. Augsburger 2008
81. Pharmaceutical Dosage Forms: Tablets, Volume 2, 2nd Ed. Herbert A. Lieberman 1990
82. Pharmaceutical Dosage Forms: Tablets, Volume 3, 2nd Ed. Herbert A.Lieberman 1990
83. Pharmaceutical Photostability and Stabilization Technology. Joseph T. Piechocki 2007
84. Pharmaceutical Powder Compaction Technology (Drugs and the Pharmaceutical Sciences). Goran
Alderborn 1996
85. Pharmaceutical Process Scale-Up (Drugs and the Pharmaceutical Sciences). Michael Levin 2002
86. Pharmaceutical Process Scale-Up, 2nd edition (Drugs and the Pharmaceutical Sciences). Michael Levin
2006
87. Pharmaceutical Technology: Controlled Drug Release, Volume 2 (Ellis Horwood Series in Pharmaceutical
Technology). James I. Wells 1991
88. Photostability of Drugs and Drug Formulations, 2nd Ed. Hanne Hjorth Tnnesen 2004
89. Photostability of Drugs and Drug Formulations. Hanne Hjorth Tnnesen 1996
90. Preformulation in Solid Dosage Form Development (Drugs and the Pharmaceutical Sciences). Moji
Christianah Adeyeye 2008
91. Principles of Polymer Science and Technology in Cosmetics and Personal Care. E. Desmond Goddard
1999
92. Protein-Based Films and Coatings. Aristippos Gennadios 2002.
93. Rheology Essentials of Cosmetic and Food Emulsions. Rudiger Brummer 2006
94. Skin Moisturization (Cosmetic Science and Technology Series). James J. Leyden 2002
95. Stability of Drugs and Dosage Forms. Sumie Yoshioka 2002
96. Tablet And Capsule Machine Instrumentation. Peter Ridgway Watt 2008
97. The Chemistry and Physics of Coatings. A.R. Marrion 2004
98. Topical Absorption of Dermatological Products (Basic and Clinical Dermatology). Robert L. Bronaugh 2002
99. Transdermal Drug Delivery, Second Edition, (Drugs & the Pharmaceutical Sciences). Jonathan Hadgraft
2003
100. Vademecum for Vitamin Formulations, 2nd Ed. Volker Buhler 2001

Bonus:

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
Daftar E-book DVD Kompilasi Industri 3

1. 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 OBrien 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 Users 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. Wileys Remediation Technologies Handbook: Major Contaminant Chemicals and Chemical Groups. Jay
H Lehr 2004.

Bonus:

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
Daftar E-book DVD Kompilasi Industri 4

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 2007 (United States Pharmacopeia 30 / National Formulary 25)
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. Jrg 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 Lpez 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 Bivre 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

Bonus:

1. British Pharmacopoeia 2007


2. Perundangan Kesehatan dan Keselamatan Kerja (K3) - ISO 17025
3. CleanRooms - Magazines Maret 2008
4. CleanRooms - Magazines April 2008
5. CleanRooms - Magazines Mei 2008
Daftar E-book Industri 5

1. High-Performance Thin-Layer Chromatography (HPTLC). ManMohan Srivastava 2011


2. Handbook of HPLC, 2nd Ed (Chromatographic Science Series, Vol 101). Danilo Corradini 2011
3. Handbook of Pharmaceutical Manufacturing Formulations, 2nd Ed, Vol 1: Compressed Solid Products.
Sarfaraz K. Niazi 2009
4. Handbook of Pharmaceutical Manufacturing Formulations, 2nd Ed, Vol 2: Uncompressed Solid Products.
Sarfaraz K. Niazi 2009
5. Handbook of Pharmaceutical Manufacturing Formulations, 2nd Ed, Vol 5: Over-the-Counter Products.
Sarfaraz K. Niazi 2009
6. Handbook of Isolation and Characterization of Impurities in Pharmaceuticals (Separation Science and
Technology). Satinder Ahuja 2003
7. Handbook of Non-Invasive Drug Delivery Systems (Personal Care and Cosmetic Technology). Vitthal S.
Kulkarni 2010
8. Handbook of Pharmaceutical Generic Development, Vol 1- Tablet Oral: Part I (Development). Locum
International Publishing 2000
9. Handbook of Pharmaceutical Granulation Technology, 3rd Ed (Drugs and the Pharmaceutical Sciences, Vol
198). Dilip M. Parikh 2010
10. Handbook Good Laboratory Practice (GLP), 1st Ed: Quality practices for regulated non-clinical research and
development. UNDP/World Bank/WHO 2001
11. Handbook Good Laboratory Practice (GLP), 2nd Ed: Quality practices for regulated non-clinical research
and development.UNDP/World Bank/WHO 2009
12. Handbook of Cosmetic Skin Care, 2nd Ed. Avi Shai 2009
13. Encyclopedia of Analytical Chemistry: Applications, Theory, and Instrumentation. Robert A. Meyers 2001
14. Encyclopedia of Analytical Science, 2nd Ed (10 Vol Set). Paul Worsfold 2004
15. Encyclopedia of Chromatography, 3rd Ed ( Vol I,II and III). Jack Cazes 2010
16. Encyclopedia of Separation Science (10 Vol Set). Michael Cooke 2000
17. Leung's Encyclopedia of Common Natural Ingredients: Used in Food, Drugs and Cosmetics, 3rd Ed. Ikhlas
A. Khan 2010
18. A Guide to Pharmaceutical Particulate Science. Timothy M. Crowder 2003
19. Advanced Drug Formulation Design to Optimize Therapeutic Outcomes (Drugs and the Pharmaceutical
Sciences, Vol 172). Robert O. Williams III 2008
20. Agglomeration Processes: Phenomena, Technologies, Equipment. Wolfgang B. Pietsch 2002
21. Analytical Chemistry for Technicians, 3rd Ed. John Kenkel 2003
22. Antiperspirants and Deodorants, 2nd Ed (Cosmetic Science and Technology Series). Karl Laden 1999
23. Bioengineering of the Skin: Skin Imaging & Analysis, 2nd Ed. Klaus-Peter Wilhelm 2007
24. Bioengineering of the Skin: Water and the Stratum Corneum, 2nd Ed. Joachim Fluhr 2005
25. Biotechnology in Personal Care. Raj Lad 2006.
26. Buying and Selling Laboratory Instruments: A Practical Consulting Guide. Marvin C. McMaster 2010
27. Characterisation of Bulk Solids. Don McGlinchey 2005
28. Chemical and Physical Behavior of Human Hair, 4th Ed. Clarence R. Robbins 2001
29. Cosmeceuticals and Active Cosmetics: Drugs Versus Cosmetics, 2nd Ed. Peter Elsner 2005
30. Cosmeceuticals: Drugs Versus Cosmetics, 1st Ed. Peter Elsner 2000
31. Cosmetic Claims Substantiation (Cosmetic Science and Technology Series). Louise Aust 1997
32. Cosmetic Dermatology: Products and Procedures. Zoe Diana Draelos 2010
33. CRC Handbook of Laboratory Safety, 5th Ed. A. Keith Furr 2000
34. Current Protocols Essential Laboratory Techniques. Sean R. Gallagher 2008
35. Dermal Absorption and Toxicity Assessment, 2nd Ed (Drugs and the Pharmaceutical Sciences, Vol 177).
Michael S. Roberts 2008
36. Dry Skin and Moisturizers: Chemistry and Function, 2nd Ed. Marie Loden 2006
37. Extraction Techniques in Analytical Sciences. John R. Dean 2009
38. FASTtrack: Pharmaceutics-Drug Delivery and Targeting. Yvonne Perrie 2010
39. FASTtrack: Physical Pharmacy. David Attwood 2008
40. Global Regulatory Issues for the Cosmetics Industry, Vol 1. C.I. Betton 2007
41. Hair and Hair Care (Cosmetic Science and Technology Series). Dale H. Johnson 1997
42. Hazardous Laboratory Chemicals Disposal Guide, 3rd Ed. Margaret-Ann Armour 2003
43. Imaging Mass Spectrometry: Protocols for Mass Microscopy. Mitsutoshi Setou 2010
44. Introduction to Modern Liquid Chromatography, 3rd Ed. Lloyd R. Snyder 2010
45. Laboratory Design Guide, 3rd Ed. Brian Griffin 2005
46. Laboratory Design, Construction, and Renovation: Participants, Process, and Product. National Academy of
Sciences 2000
47. Manual of Basic Techniques for a Health Laboratory, 2nd Ed. WHO 2003
48. Manual on Test Sieving Methods: Guidelines for Establishing Sieve Analysis Procedures, 4th Ed (Astm
Manual Series). Lawrence R. Pope 1998
49. Modelling of Powder Die Compaction. Peter R. Brewin 2008
50. Multifunctional Cosmetics. Randy Schueller 2003
51. New Cosmetic Science. Takeo Mitsui 1993
52. Oral Drug Absorption: Prediction and Assessment (Drugs and the Pharmaceutical Sciences, Vol 106).
Jennifer B. Dressman 2000
53. Oral Drug Absorption: Prediction and Assessment, 2nd Ed (Drugs and the Pharmaceutical Sciences, Vol
193). Jennifer B. Dressman 2010
54. Particle Size Measurement, 5th Ed, Vol 1: Powder Sampling and Particle Size Measurement (Particle
Technology Series). Terence Allen 1997
55. Particle Size Measurement, 5th Ed, Vol 2: Surface Area and Pore Size Determination (Particle Technology
Series). Terence Allen 1997
56. Particle Size Measurements: Fundamentals, Practice, Quality (Particle Technology Series). Henk G. Merkus
2009
57. Pediatric Drug Development: Concepts and Applications. Andrew E. Mulberg 2009
58. Perfumery: Practice and Principles. Robert R. Calkin 1994
59. Pharmaceutical Product Development: In Vitro-In Vivo Correlation (Drugs and the Pharmaceutical Sciences,
Vol 165). Dakshina Murthy Chilukuri 2007
60. Pharmaceutical Stability Testing to Support Global Markets (Biotechnology: Pharmaceutical Aspects, Vol
XII). Kim Huynh-Ba 2010
61. Physical Characterization of Pharmaceutical Solids (Drugs and the Pharmaceutical Sciences, Vol 70). Harry
G. Brittain 1995
62. Polymorphism in Pharmaceutical Solids, 2nd Ed (Drugs and the Pharmaceutical Sciences, Vol 192). Harry
G. Brittain 2009
63. Polymorphism in Pharmaceutical Solids. Harry G. Brittain 1999
64. Polymorphism in the Pharmaceutical Industry. Rolf Hilfiker 2006
65. Poucher's Perfumes, Cosmetics and Soaps, 10th Ed. Hilda Butler 2000
66. Powder Technology Handbook, 2nd Ed. Keishi Gotoh 1997
67. Powder Technology Handbook, 3rd Ed. Hiroaki Masuda 2006
68. Powder Technology: Fundamentals of Particles, Powder Beds, and Particle Generation (Powder Technology
Series). Hiroaki Masuda 2007
69. Powder Technology: Handling and Operations, Process Instrumentation, and Working Hazards (Powder
Technology Series). Hiroaki Masuda 2007
70. Powder Testing Guide: Methods of Measuring the Physical Properties of Bulk Powders. L. Svarovskly 1987
71. Powders and Bulk Solids: Behavior, Characterization, Storage and Flow. Dietmar Schulze 2008
72. Practical Aspects of Cosmetic Testing: How to Set up a Scientific Study in Skin Physiology. Joachim W.
Fluhr 2011
73. Practical High-Performance Liquid Chromatography, 5th Ed. Veronika R. Meyer 2010
74. Preclinical Drug Development, 2nd Ed (Drugs and the Pharmaceutical Sciences, Vol 187). Mark C. Rogge
2010
75. Preparative Chromatography of Fine Chemicals and Pharmaceutical Agents. Henner Schmidt-Traub 2005
76. Preservative-free and Self-preserving Cosmetics and Drugs (Principles and Practices, Cosmetic Science
and Technology Series, Vol 16). Jon J. Kabara 1997
77. Process Analytical Technology: Spectroscopic Tools and Implementation Strategies for the Chemical and
Pharmaceutical Industries, 2nd Ed. Katherine A. Bakeev 2010
78. Process Analytical Technology: Spectroscopic Tools and Implementation Strategies for the Chemical and
Pharmaceutical Industries. Katherine A. Bakeev 2005
79. Process Chemistry in the Pharmaceutical Industry, Vol 2: Challenges in an Ever Changing Climate. Kumar
G. Gadamasetti 2008
80. Process Chemistry in the Pharmaceutical Industry. Kumar G. Gadamasetti 1999
81. Profiles of Drug Substances, Excipients and Related Methodology, Vol 34. Harry G. Brittain 2009
82. Safety Assessment of Cosmetics in Europe (Current Problems in Dermatology, Vol 36). Vera Rogiers 2008
83. Skin Aging Handbook: An Integrated Approach to Biochemistry and Product Development (Personal Care
and Cosmetic Technology). Nava Dayan 2008
84. Soap Manufacturing Technology. Luis Spitz 2009
85. Soaps, Detergents, Oleochemicals, and Personal Care Products. Luis Spitz 2004.
86. Steroid Analysis, 2nd Ed. Hugh L.J. Makin 2010
87. Sunscreens: Development, Evaluation, and Regulatory Aspects, 2nd Ed. Nicholas J. Lowe 1996
88. Sunscreens: Regulations and Commercial Development, 3rd Ed (Cosmetic Science and Technology
Series). Nadim A. Shaath 2005
89. Surfactants in Cosmetics, 2nd Ed. Martin M. Rieger 1997
90. Surfactants in Personal Care Products and Decorative Cosmetics, 3rd Ed. Linda D. Rhein 2007
91. The Chemistry of Fragrances. David H.Pybus 1999
92. The Chemistry of Fragrances: From Perfumer to Consumer, 2nd Ed. By Charles Sell 2006
93. The Complete Idiot's Guide to Making Natural Soaps. Sally W. Trew 2010
94. The HPLC Solvent Guide, 2nd Ed. Paul C. Sadek 2002
95. The Laboratory Companion : A Practical Guide to Materials, Equipment, and Technique. G. S. Coyne 1997
96. The Science of Hair Care, 2nd Ed. Claude Bouillon 2005
97. Transport Processes in Pharmaceutical Systems (Drugs and the Pharmaceutical Sciences, Vol 102).
Gordon L. Amidon 2000
98. Valid Analytical Methods and Procedures. Christopher Burgess 2001
99. Validating Chromatographic Methods: A Practical Guide. David M. Bliesner 2006
100. Vogel's Qualitative Inorganic Analysis, 7th Ed. G. Svehla 1996

Bonus

1. A New Approach to Lower Limits of Detection and Easy Spectral Analysis: Applications of Fluorescence
Detection in Liquid Chromatography (Agilent Publication). Rainer Schuster 2000
2. Analytical Instrument Qualification and System Validation (Agilent Publication). Ludwig Huber 2009
3. Basic Tests for Drugs: Pharmaceutical Substances, Medicinal Plant Materials and Dosage Forms. WHO
1998
4. Basic Tests for Pharmaceutical Dosage Forms. WHO 1991
5. Basic Tests for Pharmaceutical Substances. WHO 1986
6. Electrochemical Detection in High Performance Liquid Chromatography: A Practical Primer. Hewlett-
Packard 1989
7. Fundamentals of UV-visible spectroscopy: Primer (Agilent Publication). Agilent Technologies, Inc 2000
8. Fundamentals of UV-visible spectroscopy: Workbook (Agilent Publication). Agilent Technologies, Inc 2000
9. Good Laboratory Practice and Current Good Manufacturing Practice (Agilent Publication). Ludwig Huber
2002
10. Guideline on Stability Testing: Stability Testing of Existing Active Substances and Related Finished
Products. EMEA 2003
11. ICP-MS Inductively Coupled Plasma Mass Spectrometry (Agilent Publication). Agilent Technologies, Inc
2005
12. Principles in Preparative HPLC (Agilent Publication). Udo Huber 2007
13. The Handbook of Soap Manufacture. W.H. Simmons 1908
14. Validation of Analytical Methods (Agilent Publication). Ludwig Huber 2010
15. Pure Health Magazine : The World of Personal Care Ingredients. 2009-2010
16. Video - A Brief Guide to HPLC Instruments. Mourne Training Services
17. Video - Basic Laboratory Techniques. The Chinese University of Hong Kong - Department of Chemistry
18. Video - Clear Automation Automated Cosmetic Manufacturing
19. Video - Column Chromatography. Departement of Chemistry Massachusetts Institute of Technology
20. Video - Contoh Analisis Cyclofem dengan HPLC
21. Video - GC Troubleshooting (Agilent Instructional)
22. Video - How Its Made Cosmetics
23. Video - How Soap Bars is Made
24. Video - How Toothpaste Is Made
25. Video - Introduction to Volumetric Glassware. David Frank
26. Video - Optimizing your LC for Rapid Resolution High Throughput (Agilent Instructional)
27. Video - Pills How its made
28. Video - Tablet Manufacturing Process
Daftar E-book Industri 6

1. Handbook of Pharmaceutical Manufacturing Formulations, 2nd Ed, Vol 3: Liquid Products. S. K. Niazi 2009
2. Handbook of Pharmaceutical Manufacturing Formulations, 2nd Ed, Vol 4: Semisolid Products. S. K. Niazi
2009
3. Handbook of Pharmaceutical Manufacturing Formulations, 2nd Ed, Vol 6: Sterile Products. S. K. Niazi 2009
4. Handbook of Solubility Data for Pharmaceuticals. Abolghasem Jouyban 2010
5. Handbook of Acid-Base Indicators. R. W. Sabnis 2008
6. Handbook of Chemical Compound Data for Process Safety. Carl L. Yaws 1997
7. Handbook of Drug Screening, 2nd Ed (Drugs and the Pharmaceutical Sciences, Vol 196). Ramakrishna
Seethala 2009
8. Handbook of Hazardous Chemical Properties. Nicholas P. Cheremisinoff 2000
9. Handbook of Membrane Separations: Chemical, Pharmaceutical, Food, and Biotechnological Applications.
Anil K. Pabby 2009
10. Handbook of Microbiological Media, 4th Ed. Ronald M. Atlas 2010
11. Handbook of Microbiological Quality Control in Pharmaceuticals and Medical Devices (Taylor & Francis
Series in Pharmaceutical Sciences). Rosamund M. Baird 2000
12. Handbook of Organic Solvent Properties. Ian M. Smallwood 1996
13. Handbook of Solvents. George Wypych 2001
14. Ullmann's Encyclopedia of Industrial Chemistry,6th Ed (40 Volume Set). Fritz Ullmann 2003
15. A Guide to Safe Material and Chemical Handling. Nicholas P. Cheremisinoff 2010
16. A Working Guide to Process Equipment, 3rd Ed. Norman P. Lieberman 2008
17. Advanced Cleaning Product Formulations (5 Vol Set). Ernest W. Flick 1999
18. Air Sampling and Industrial Hygiene Engineering. Martha J. Boss 2001.
19. Batch Chemical Process Integration: Analysis, Synthesis and Optimization. Thokozani Majozi 2010
20. Batch Distillation: Design and Operation. I. M. Mujtaba 2004
21. Batch Fermentation: Modeling, Monitoring, and Control. Ali Cinar 2003
22. Biocatalysis for the Pharmaceutical Industry: Discovery, Development, and Manufacturing. Junhua Tao 2009
23. Biodrug Delivery Systems: Fundamentals, Applications and Clinical Development (Drugs and the
Pharmaceutical Sciences, Vol 194). Mariko Morishita 2010
24. Bubbles, Drops, and Particles in Non-Newtonian Fluids, 2nd Ed. R. P. Chhabra 2007
25. Chemical Process Equipment: Selection and Design, 3rd Ed. James R. Couper 2010
26. Cleaning Validation Manual: A Comprehensive Guide for the Pharmaceutical and Biotechnology Industries.
Syed Imtiaz Haider 2010
27. Cleanroom Microbiology for the Non-Microbiologist 2nd ed. David M. Carlberg 2005
28. Coagulation and Flocculation, 2nd Ed (Surfactant Science). Hansjoachim Stechemesser 2005
29. Colloid Science: Principles, Methods and Applications, 2nd Ed. Terence Cosgrove 2010
30. Colloids in Drug Delivery (Surfactant Science, Vol 148). Monzer Fanun 2010
31. Coloring of Food, Drugs, and Cosmetics. Otterstatter 1999
32. Compatibility of Pharmaceutical Products and Contact Materials: Safety Considerations Associated with
Extractables and Leachables. Dennis Jenke 2009
33. Containment in the Pharmaceutical Industry (Drugs and the Pharmaceutical Sciences, Vol 108). James P.
Wood 2001
34. Contamination Control in Practice: Filtration and Sterilisation. Matts Ramstorp 2003
35. Co-Rotating Twin Screw Extruders: Fundamentals, Technology, and Applications. Klemens Kohlgruber 2008
36. Delivery Technologies for Biopharmaceuticals: Peptides, Proteins, Nucleic Acids and Vaccines. Lene
Jorgensen 2009
37. Design & Development of Biological, Chemical, Food and Pharmaceutical Products. Johannes A.
Wesselingh 2007
38. Developments in Surface Contamination and Cleaning, Vol 2. Rajiv Kohli 2010
39. Discrete Time Analysis of Batch Processes in Material Flow Systems. Marc Schleyer 2007
40. Dust Control Handbook (Pollution Technology Review). Vinit Mody 1988
41. Emulsions, Foams, and Suspensions: Fundamentals and Applications. Laurier L. Schramm 2005
42. Engineering Data on Mixing. Reiji Mezaki 2000
43. Facility Piping Systems Handbook: For Industrial, Commercial, and Healthcare Facilities, 3rd Ed. Michael
Frankel 2010
44. Formulation and Process Development Strategies for Manufacturing Biopharmaceuticals. Feroz Jameel
2010
45. Freeze-Drying/Lyophilization Of Pharmaceutical & Biological Products, 3rd Ed (Drugs and the
Pharmaceutical Sciences, Vol 206). Louis Rey 2010
46. Gardner's Commercially Important Chemicals: Synonyms, Trade Names, and Properties. G. W. A. Milne
2005
47. Gelatine Handbook: Theory and Industrial Practice. Reinhard Schrieber 2007
48. Green Chemistry in the Pharmaceutical Industry. Peter J. Dunn 2010
49. Guide to Microbiological Control in Pharmaceuticals and Medical Devices, 2nd Ed. Stephen P. Denyer 2007
50. Industrial Boilers and Heat Recovery Steam Generators: Design, Applications, and Calculations. V.
Ganapathy 2003
51. Industrial Drying Equipment: Selection and Application. C.M. Van 't Land 1991
52. Industrial Machinery Repair: Best Maintenance Practices Pocket Guide. Ricky Smith 2003
53. Industrial Solvents Handbook, 2nd Ed. Nicholas P. Cheremisinoff 2003
54. Industrial Solvents Handbook, 5th Ed. Ernest W. Flick 1998
55. Introduction to Contamination Control and Cleanroom Technology. Matts Ramstorp 2000
56. Lyophilization: Introduction and Basic Principles. Thomas A. Jennings 2008
57. Manufacturing of Pharmaceutical Proteins: From Technology to Economy. Stefan Behme 2009
58. Micro and Macro Mixing: Analysis, Simulation and Numerical Calculation. Henning Bockhorn 2010
59. Mixing in Single Screw Extrusion. Martin Gale 2009
60. Mixing in the Process Industries, 2nd Ed. N. Harnby 1992
61. Modern Pharmaceutics, Fifth Edition, Volume 1: Basic Principles and Systems (Drugs and the
Pharmaceutical Sciences, Vol 188). Alexander T. Florence 2009
62. Moisture Control in Buildings: The Key Factor in Mold Prevention, 2nd Ed. Heinz R. Trechsel 2009
63. Multilayer Flexible Packaging: Technology and Applications for the Food, Personal Care, and Over-The-
Counter Pharmaceutical Industries. John R. Wagner Jr 2010
64. Pharmaceutical Biotechnology, 2nd Ed. Michael J. Groves 2006
65. Pharmaceutical Data Mining: Approaches and Applications for Drug Discovery (Wiley Series on
Technologies for the Pharmaceutical Industry). Konstantin V. Balakin 2010
66. Pharmaceutical Packaging Handbook. Edward J. Bauer 2009
67. Pharmaceutical Preformulation and Formulation: A Practical Guide from Candidate Drug Selection to
Commercial Dosage Form, 2nd Ed (Drugs and the Pharmaceutical Sciences, Vol 199). Mark Gibson 2009
68. Pharmaceutical Preformulation. Jens T. Carstensen 1998
69. Pharmaceutical Process Engineering, 2nd Ed (Drugs and the Pharmaceutical Sciences, Vol 195). Anthony
J. Hickey 2010
70. Pharmaceutical Suspensions: From Formulation Development to Manufacturing. Alok K. Kulshreshtha 2010
71. Polyvinylpyrrolidone Excipients for Pharmaceuticals: Povidone, Crospovidone and Copovidone. Volker
Bhler 2005
72. Practical Batch Process Management. Mike Barker 2005
73. Process Validation in Manufacturing of Biopharmaceuticals: Guidelines, Current Practices, and Industrial
Case Studies. Anurag Singh Rathore 2005.
74. Protein Formulation and Delivery (Drugs and the Pharmaceutical Sciences, Vol 99). Eugene J. McNally
2000
75. Protein Formulation and Delivery, 2nd Ed (Drugs and the Pharmaceutical Sciences, Vol 175). Eugene J.
McNally 2008
76. Reverse Osmosis: Design, Processes, and Applications for Engineers. Jane Kucera 2010
77. Rheology Modifiers Handbook:Practical Use and Application. David B. Braun 2000
78. Rheology of Complex Fluids. Abhijit P. Deshpande 2010
79. Rheology of Dispersions: Principles and Applications. Tharwat F. Tadros 2010
80. Rheometry of Pastes, Suspensions, and Granular Materials: Applications in Industry and Environment.
Philippe Coussot 2005
81. Safe Use of Chemicals: A Practical Guide. T.S.S. Dikshith 2009
82. Solvent Extraction Principles and Practice, 2nd Ed. Jan Rydberg 2004
83. Solvent Systems and Their Selection in Pharmaceutics and Biopharmaceutics (Biotechnology:
Pharmaceutical Aspects, Vol VI). Patrick Augustijns 2007
84. Sterile Filtration (Advances in Biochemical Engineering / Biotechnology, Vol 98). Maik W. Jornitz 2006
85. Sterilization Validation and Routine Operation Handbook: Ethylene Oxide. Anne F. Booth 2000
86. Stirring: Theory and Practice. Marko Zlokarnik 2001
87. Surface Contamination and Cleaning, Volume 1. K.L. Mittal 2003
88. Tank Linings for Chemical Process Industries. V. C. Chandrasekaran 2009
89. The Effect of Sterilization Methods on Plastics and Elastomers, 2nd Ed. Liesl K. Massey 2005
90. The Kinematics of Mixing: Stretching, Chaos, and Transport. J. M. Ottino 1989
91. The Nalco Water Handbook, 3rd Ed. Daniel J. Flynn 2009
92. The Science and Technology of Industrial Water Treatment. Zahid Amjad 2010
93. The Structure and Rheology of Complex Fluids. Ronald G. Larson 1999
94. The Wiley Encyclopedia of Packaging Technology, 3rd Ed. Kit L. Yam 2009
95. Troubleshooting the Sequencing Batch Reactor (Wastewater Microbiology). Michael H. Gerardi 2010
96. Validation of Pharmaceutical Processes: Sterile Products, 2nd Ed. Frederick J. Carleton 1998
97. Verification, Validation and Testing of Engineered Systems. Avner Engel 2010
98. Water Properties in Food, Health, Pharmaceutical and Biological Systems. D. S. Reid 2010
99. White's Handbook of Chlorination and Alternative Disinfectants, 5th Ed. Black & Veatch Corp 2010
100. Wiley Guide to Chemical Incompatibilities, 3rd Ed. Richard P. Pohanish 2009

Bonus

1. Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms, 2nd Ed (Drugs and the Pharmaceutical
Sciences, Vol 79). James W. McGinity 1997
2. Cleanrooms and Associated Controlled Environments Part 1: Classification of Air Cleanliness(ISO 14644-
1:1999). ISO 1999
3. Cleanrooms and Associated Controlled Environments Part 2: Specifications for Testing and Monitoring to
Prove Continued Compliance with ISO 14644-1(ISO 14644-2:2000). ISO 2000
4. Cleanrooms and Associated Controlled Environments Part 4: Design, Construction and Start-up (ISO
14644-4:2001). ISO 2001
5. Cleanrooms and Associated Controlled Environments Part 5: Operations (ISO 14644-5:2004). ISO 2004
6. Cleanrooms and Associated Controlled Environments Part 7: Separative Devices (Clean air hoods,
gloveboxes, isolators and minienvironments)(ISO 14644-7:2004). ISO 2004
7. Cleanrooms and Associated Controlled Environments Part 8: Classification of Airborne Molecular
Contamination (ISO 14644-8:2006). ISO 2006
8. Cleanrooms and Associated Controlled Environments-Biocontamination control - Part 2: Evaluation and
interpretation of biocontamination data (ISO 14698-2:2003). ISO 2003
9. Endotoxins: Pyrogens, LAL Testing and Depyrogenation, 2nd Ed (Drugs and the Pharmaceutical Sciences,
Vol 111 ). Kevin L. Williams 2001
10. Guidance for Industry Nonsterile Semisolid Dosage Forms: Scale-Up and Postapproval Changes:
Chemistry, Manufacturing, and Controls; In Vitro Release Testing and In Vivo Bioequivalence
Documentation. FDA 1997
11. Guidance for Industry Sterile Drug Products: Produced by Aseptic Processing Current Good
Manufacturing Practice. FDA 2004
12. Health Technical Memorandum 2010 - Sterilization. NHS 1994
13. Pharmaceutical Process Validation, 2nd Ed (Drugs and the Pharmaceutical Sciences, Vol 57). Ira R. Berry
1993
14. Primary Packaging Materials for Medicinal Products (ISO 15378:2006): Particular requirements for the
application of ISO 9001:2000, with reference to Good Manufacturing Practice (GMP). ISO 2006
15. Lab Manager Magazine : Where Science and Management Meet. 2006 - 2010
16. Video - Analytical Method Development for Cleaning Validation. Steven Institute of Technology
17. Video - Blister Packing Line
18. Video - Encap Drug Delivery Capsule Filling Process
19. Video - How Condoms Are Made
20. Video - Medicine Capsule Manufacturing
21. Video - Modul WOL (Wash-Off-Line) concept
22. Video - Softgel Encapsulation Machine
23. Video - Sterilization and Disinfection. Indira Gandhi National Open University
24. Video - Syrup Manufacturing Process
Daftar E-book Industri 7

1. Safety Evaluation of Pharmaceuticals and Medical Devices: International Regulatory Guidelines. Shayne
C. Gad 2011
2. Monte Carlo Simulation for the Pharmaceutical Industry: Concepts, Algorithms, and Case Studies. Mark
Chang 2011
3. JIT Implementation Manual: The Complete Guide to Just-In-Time Manufacturing, 2nd Ed, Vol 1- The Just
in Time Production System. Hiroyuki Hirano 2009
4. JIT Implementation Manual: The Complete Guide to Just-In-Time Manufacturing, 2nd Ed, Vol 2- Waste
and the 5S's. Hiroyuki Hirano 2009
5. JIT Implementation Manual: The Complete Guide to Just-In-Time Manufacturing, 2nd Ed, Vol 3- Flow
Manufacturing Multi Process Operations and Kanban. Hiroyuki Hirano 2009
6. JIT Implementation Manual: The Complete Guide to Just-In-Time Manufacturing, 2nd Ed, Vol 4- Leveling
Changeover and Quality Assurance. Hiroyuki Hirano 2009
7. JIT Implementation Manual: The Complete Guide to Just-In-Time Manufacturing, 2nd Ed, Vol 5-
Standardized Operations-Jidoka and Maintenance/Safety. Hiroyuki Hirano 2009
8. JIT Implementation Manual: The Complete Guide to Just-In-Time Manufacturing, 2nd Ed, Vol 6- JIT
Implementation Forms and Charts. Hiroyuki Hirano 2009
9. ISO 9001:2008 for Small Businesses, 4th Ed. Ray Tricker 2010
10. A Model Quality Assurance System for Procurement Agencies: Recommendations for Quality Assurance
Systems Focusing on Prequalification of Products and Manufacturers, Purchasing, Storage and
Distribution of Pharmaceutical Products. WHO 2007
11. A Roadmap to Quality: An e-learning Manual for Implementing Total Quality Management (2 Vol Set).
United Nations Industrial Development Organization (UNIDO) 2007
12. A WHO guide to good manufacturing practice requirements, Part 1: Standard Operating Procedures and
Master Formulae (Global Programme for Vaccines and Immunization). WHO 1997
13. A WHO guide to good manufacturing practice requirements, Part 2: Validation (Global Programme for
Vaccines and Immunization). WHO 1997
14. A WHO guide to good manufacturing practice requirements, Part 3: Training (Global Programme for
Vaccines and Immunization). WHO 2006
15. Acceptance Sampling in Quality Control, 2nd Ed. Edward G. Schilling 2008
16. Australian Code of Good Manufacturing Practice for Medicinal Products. TGA 2002
17. Australian Code of Good Manufacturing Practice: Human Blood and Tissues. TGA 2000
18. Best Practices of ISO 14021: Self-Declared Environmental Claims. Kun-Mo Lee 2003
19. Complying with ISO 17025: A Practical Guidebook for Meeting the Requirements of Laboratory
Accreditation Schemes Based on ISO 17025:2005 or Equivalent National Standards. UNIDO 2009
20. Electronic Record Keeping: Achieving and Maintaining Compliance wih 21 CFR Part 11 and 45 CFR parts
160, 162, and 164. David Nettleton 2004
21. Environmental Management Plans Demystified: A Guide to ISO 14001. Stephen Tinsley 2001
22. Excellence in Warehouse Management: How to Minimise Costs and Maximise Value. Stuart Emmett 2005
23. Excipient Toxicity and Safety (Drugs and the Pharmaceutical Sciences, Vol 103). Myra L. Weiner 2000
24. Global Pharmaceutical Policy: Ensuring Medicines for Tomorrow's World. Frederick M. Abbott 2009
25. Guide to Good Manufacturing Practice for Medicinal Products. PIC/S 2009
26. Guidelines for Chemical Process Quantitative Risk Analysis, 2nd Ed. CCPS 2000
27. Guidelines for Chemical Reactivity Evaluation and Application to Process Design. CCPS 1995
28. Guidelines for Consequence Analysis of Chemical Releases. CCPS 1999
29. Guidelines for Developing Quantitative Safety Risk Criteria. Center for Chemical Process Safety 2009
30. Guidelines for Engineering Design for Process Safety. CCPS 1993
31. Guidelines for Evaluating Process Plant Buildings for External Explosions and Fires.CCPS 1996
32. Guidelines for Facility Siting and Layout. Center for Chemical Process Safety (CCPS) 2003
33. Guidelines for Failure Mode and Effects Analysis for Medical Devices. Dyadem Engineering Corp 2003
34. Guidelines for Hazard Evaluation Procedures, 2nd Ed with Worked Examples. CCPS 1992
35. Guidelines for Hazard Evaluation Procedures, 3rd Ed. Center for Chemical Process Safety 2008
36. Guidelines for Improving Plant Reliability Through Data Collection and Analysis. CCPS 1998
37. Guidelines for Integrating Process Safety Management, Environment, Safety, Health, and Quality. CCPS
1996
38. Guidelines for Mechanical Integrity Systems. CCPS 2006
39. Guidelines for Performing Effective Pre-Startup Safety Reviews. CCPS 2007
40. Guidelines for Preventing Human Error in Process Safety. CCPS 1994
41. Guidelines for Process Equipment Reliability Data, with Data Tables. CCPS 1989
42. Guidelines for Process Safety Documentation. CCPS 1995
43. Guidelines for Process Safety Fundamentals in General Plant Operations. CCPS 1995
44. Guidelines for Process Safety in Batch Reaction Systems. CCPS 1999
45. Guidelines for Process Safety in Outsourced Manufacturing Operations. CCPS 2000
46. Guidelines for Procurement of Pharmaceuticals &Medical Devices. National Procurement Agency 2006
47. Guidelines for Risk Based Process Safety. CCPS 2007
48. Guidelines for Safe and Reliable Instrumented Protective Systems. CCPS 2007
49. Guidelines for Safe Automation of Chemical Processes. CCPS 1993
50. Guidelines for Safe Process Operations and Maintenance. CCPS 1995
51. Guidelines for the Management of Change for Process Safety. CCPS 2008
52. Guidelines for the Storage of Essential Medicines and Other Health Commodities. Laurie Lyons 2003
53. Guidelines for Warehousing Health Commodities. Tim O'Hearn 2005
54. Guidelines for Writing Effective Operating and Maintenance Procedures. CCPS 1996
55. Health, Safety and Accident Management in the Chemical Process Industries. Ann Marie Flynn 2002
56. Human Factors Methods for Improving Performance in the Process Industries.CCPS 2007
57. Implementing Quality in Laboratory Policies and Processes: Using Templates, Project Management, and
Six Sigma. Donnell R. Christian, Jr. 2010
58. Implementing the ISO 14001 Environmental Management System Specification, Version 2.0. James H.
Schaarsmith 2005
59. Improving Inventory Record Accuracy: Getting your stock information right. Tony Wild 2004
60. International Biotechnology, Bulk Chemical, and Pharmaceutical GMPs, 5th Ed. Michael H. Anisfeld 2002
61. Lee's Loss Prevention in the Process Industries: Hazard Identification, Assessment and Control, 3rd Ed (3
Vol Set). Sam Mannan 2005
62. Managing the Documentation Maze: Answers to Questions You Didnt Even Know to Ask. J. Gough 2010
63. Measurement and Internal Audit. Andrew Fight 2002
64. Medical Device Quality Assurance and Regulatory Compliance. Richard C. Fries 1998
65. Medical Device Regulations : Global Overview and Guiding Principles. WHO 2003
66. Medical Product Regulatory Affairs: Pharmaceuticals, Diagnostics, Medical Devices. John J. Tobin 2008
67. Modern Pharmaceutical Industry: A Primer. Thomas M. Jacobsen 2010
68. Multi-Plant Safety and Security Management in the Chemical and Process Industries. G. L.L. Reniers
2010
69. Multiple Testing Problems in Pharmaceutical Statistics. Alex Dmitrienko 2010
70. New Drug Approval Process, 4th Ed: Accelerating Global Registrations (Drugs and the Pharmaceutical
Sciences, Vol 139). Richard Guarino 2004
71. New Drug Approval Process, 5th Ed (Drugs and the Pharmaceutical Sciences, Vol 190). R. A. Guarino
2009
72. Pharmaceutical and Biomedical Project Management in a Changing Global Environment. S. D. Babler
2010
73. Pharmaceutical Statistics: Practical and Clinical Applications, 5th Ed (Drugs and the Pharmaceutical
Sciences, Vol 203). Sanford Bolton 2010
74. Pharmaceuticals-where's the Brand Logic?: Branding Lessons and Strategy. Giles David Moss 2007
75. Portfolio, Program, and Project Management in the Pharmaceutical and Biotechnology Industries. Pete
Harpum 2010
76. Practical Guide to Chemical Safety Testing (Rapra Practical Guides). D J Knight 2003
77. Practical Guide to Industrial Safety: Methods for Process Safety Professionals. N. P. Cheremisinoff 2001
78. Practical Guidelines on Pharmaceutical Procurement for Countries with Small Procurement Agencies.
WHO 2002
79. Quality Assurance and Quality Control in the Analytical Chemical Laboratory. Piotr Konieczka 2009
80. Quality Assurance in Analytical Chemistry: Training and Teaching, 2nd Ed. Bernd W. Wenclawiak 2010
81. Regulating Chemical Risks: European and Global Challenges. Johan Eriksson 2010
82. Safety and Security Review for the Process Industries: Application of HAZOP, PHA and What-If Reviews,
2nd Ed. Dennis P. Nolan 2008
83. Safety Lifecycle Management in the Process Industries : The Development of a Qualitative Safety-Related
Information Analysis Technique. Berend Knegtering. 2002
84. Selecting the Right Manufacturing Improvement Tools: What Tool? When?. Ron Moore 2007
85. Time Continuity in Discrete Time Models: New Approaches for Production Planning in Process Industries.
Christopher Suerie 2005
86. Total Productive Maintenance: Proven Strategies and Techniques to Keep Equipment Running at Peak
Efficiency. Steven Borris 2006
87. Total Productivity Maintenance: A Route to World-Class Performance. Peter Willmott 2001
88. Total Quality Management: Guiding Principles for Application. Jack P. Pekar 1995
89. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 32nd Report ( WHO
Technical Report Series; 823). WHO 1992
90. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 33rd Report ( WHO
Technical Report Series; 834). WHO 1993
91. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 34th Report ( WHO Technical
Report Series; 863). WHO 1996
92. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 35th Report ( WHO Technical
Report Series; 885). WHO 1999
93. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 36th Report ( WHO Technical
Report Series; 902). WHO 2002
94. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 37th Report ( WHO Technical
Report Series; 908). WHO 2003
95. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 38th Report ( WHO Technical
Report Series; 917). WHO 2003
96. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 39th Report ( WHO Technical
Report Series; 929). WHO 2005
97. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 40th Report ( WHO Technical
Report Series; 937). WHO 2006
98. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 41st Report ( WHO Technical
Report Series; 943). WHO 2007
99. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 43rd Report ( WHO
Technical Report Series; 953). WHO 2009
100. WHO Expert Committee on Specifications for Pharmaceutical Preparations - 44th Report ( WHO Technical
Report Series; 957). WHO 2010

Bonus

1. Good Manufacturing Practices for Active Ingredient Manufacturers. EFPIA / CEFIC Working Group 1996
2. Good Manufacturing Practices: Medicinal Products for Human and Veterinary Use (The Rules Governing
Medicinal Products in the European Union, Vol 4). European Commission Directorate General III 1998
3. Guideline for Good Manufacturing Practices Inspections. Pan American Health Organization 2003
4. Guidelines for Drug Sampling: Use of the Basic Tests at the Peripheral Level. U.S. Agency for International
Development 2006
5. Guidelines for Quality and/or Environmental Management Systems Auditing (ISO 19011:2002). ISO 2002
6. Marketing Authorization of Pharmaceutical Products with Special Reference to Multisource (Generic)
Products: A Manual for Drug Regulatory Authorities. WHO 1998
7. Operational Principles for Good Pharmaceutical Procurement. WHO 1999
8. Preparing for FDA Pre-Approval Inspections (Drugs and the Pharmaceutical Sciences, Vol 93). Martin D.
Hynes 1999
9. Quality Assurance of Pharmaceuticals, Vol 1: A compendium of guidelines and related materials. WHO 1997
10. Quality management systems - Requirements (BS EN ISO 9001:2008). BSI British Standards 2008
11. Quality Management Systems: Fundamentals and vocabulary (ISO 9000:2005). ISO 2005
12. Revised Guidelines for Good Manufacturing Practice in Egypt. Central Administration of Pharmaceutical
Affairs, Ministry of Health and Population 2004
13. Understanding and Implementing ISO/IEC 17025 (Agilent Publication). Ludwig Huber 2009
14. Your Organization ISO 14001 Guidance Manual (Technical Report NCEDR/98-06). National Center for
Environmental Decision-making Research 1998
15. Pharma Magazine : The Global Magazine for the Pharmaceutical and Biopharmaceutical Industry. 2006 -
2010
16. Video - Direct to Consumer Pharmaceutical Marketing. Elizabeth Boyd UCSF School of Pharmacy
17. Video - From Molecules to Medicine
18. Video - Good Documentation Practices
19. Video - Overview of Pharmaceutical Industry Marketing Practices. Lisa Bero UCSF School of Pharmacy
20. Video - The Pharmaceutical Industry: Economics, Regulation, and Legal Issues (Northwestern Judicial
Symposium). Scott Stern May 2009
Daftar E-Book DVD Kompilasi Industri 8
1. Antiviral Drugs, WIESLAWM. KAZMIERSKI.pdf
2. Applied Statistic In Pharmaceutical Industry, Steven P Millard.pdf
3. Aqueus Solubility Data, Samuel H Y.pdf
4. British Pharmacopeia dan USP 30
5. British Pharmacopoeia 2009.pdf
6. Business and Financial Statistics Using Minitab 12 and Microsoft Excel 97, John C Lee.pdf
7. Calibration In PharmaceuticaL Laboratory, Tony Kowalski.pdf
8. Cleaning Validation Manual, Syed Imtiaz Haider.pdf
9. Dean Analytical Chemistry Handbooks, Pradyot Patnaik.pdf
10. Design and Manufacture of Pharmaceutical Tablets - Eyjolfsson, Reynir.pdf
11. Development and Validation Of Analytical Methods, Christopher Riley.pdf
12. Encyclopedia of Pharmaceutical Technology vol 20, James Swarbick.pdf
13. Excel 2007 for Scientists and Engineers, Dr. Gerard M. Verschuuren.pdf
14. Farmakope India Ayurveda
15. Good Manufacturing Practices and Inspection Quality Assurance of Pharmaceuticals,
WHO.pdf
16. Handbook of Pharmaceutical Granulation Technology,James Swarbrick.pdf
17. Introduction to Pharmaceutical Chemical Analysis.pdf
18. Introduction to Statistical Quality Control Student Resource Manual 4th Edition, Douglas C
Montgomery.pdf
19. Medicinal Chemistry, ALex Gringauz.pdf
20. Meet Minitab 15.pdf
21. Method Validation in Pharmaceutical Analysis - A Guide to Best Practice, J. Ermer and J.
H. McB. Miller.pdf
22. Organic Medical and Pharmaceutical Chemistry, John M Beale.pdf
23. Pharmaceutical Analysis A Textbook for Pharmacy Students and Pharmaceutical Chemists,
David G Watson.pdf
24. Pharmaceutical Dosage Form Vol 1, Herbert A. Lieberman.pdf
25. Pharmaceutical Dosage Forms Tablets Vol 3, Herbert A Lieberman.pdf
26. Pharmaceutical Dosage Forms Tablets, Vol. 2
27. Pharmaceutical Manufacturing Encyclopedia (3rd edition)
28. Pharmaceutical Manufacturing Encyclopedia, 2nd Edition, Marshal Sittig.pdf
29. Pharmaceutical Master Validation Plan - The Ultimate Guide to FDA, GMP, and GLP
Compliance.pdf
30. Pharmaceutical Master Validation Plan - The Ultimate Guide to FDA, GMP, and GLP
Compliance, Syed Imtiaz Haider .pdf
31. Pharmaceutical Statistics Practical and Clinical Applications Fifth Edition Drugs and the
Pharmaceutical Sciences, Sanford Bolton.pdf
32. Powder Sampling and Particle Size Determination, Terence Allen.pdf
33. Practical Statistics for the Analytical Scientist, Stephen LR Ellison.pdf
34. Practical Statistics for the Analytical Scientist.pdf
35. Qualification of HPLC.pdf
36. Qualification Validation and Verification, Pharmtech.pdf
37. Quality Assurance in Analytical Chemistry Analytical Techniques in the Sciences, Elizabeth
Prichard.pdf
38. Quantitative Data Analysis with Minitab A Guide for Social Scientists, Alan Bryman.pdf
39. Review dan Trend Analisis Bahan Baku Produk Bahan Alam 6 April.pdf
40. Six Sigma in the Pharmaceutical Industry Understanding, Reducing, and Controlling
Variation in Pharmaceuticals and Biologics, Brian K Nunnaly.pdf
41. Six Sigma Statistic with Excell and Minitab, Issa Bass.pdf
42. Six Sigma Statistics with EXCEL and MINITAB, Issa Bass.pdf
43. Statistical Analysis Microsoft Excell, Conrad Calberg.pdf
44. Statistical Methods in Analytical Chemistry Chemical Analysis A Series of Monographs on
Analytical Chemistry and Its Applications, Peter C Meier.pdf
45. Statisticians In Pharmaceutical Industry.pdf
46. Suplemen I FARMAKOPE INDONESIA EDISI IV.pdf
47. Valid Analytical Methods and Procedures, Christopher Burges.pdf
48. Validated Cleaning Technologies for Pharmaceutical Manufacturing, Destin A. LeBlanc.pdf
49. Validation and Qualification in Analytical Laboratories, Ludwig Huber.pdf
50. Validation Standard Operating Procedures,Second Edition.pdf
51. Water Properties of Food, Pharmaceutical, and Biological Materials, Maria.pdf
52. Water Quality Control Handbook, E. Robert Alley.pdf
53. WHO GMP HERBAL MEDICINE.PDF
54. WHO Monographs on Selected Medicinal Plants Vol 1&2.pdf
55. WHO monograps Medicinal Plants
56. Word and statistic for Pharmacist, Andy Eko.pdf
Daftar E-Book DVD Kompilasi Industri 9
1. Analytical Instrument Qualification and System Validation, Ludwig Huber.pdf
2. Ansel Pharmacetical Dosage Form and Drug Delivery System, Loyd Allen.pdf
3. Cleaning Validation Swab test.pdf
4. Cleanroom Design 2nd Ed, W Whyte.pdf
5. Essensial Of Pharmaceutical Preformulation, Simon Gaisford.pdf
6. Facility Validation, Graham C Wrigley.pdf
7. Farmakope India
8. FORMULATION AND PROCESS DEVELOPMENT STRATEGIES FOR MANUFACTURING
BIOPHARMACEUTICALS, Feroz Jameel.pdf
9. Freeze Dring in Pharmaceutical and Biopharmaceuticals, Felix Franks.pdf
10. Good Laboratory Practices, WHO.pdf
11. Good Manufacturing Practises for Pharmaceutical 6th, Joseph Nally.pdf
12. Handbook of Paper and Board, Herbert Holik.pdf
13. Handbook of Pharmaceutical Analysis, Lena Ohannesian.pdf
14. Handbook of Pharmaceutical Excipients Rowe Handbook of Pharmaceutical Excipients,
Raymond Rowe.pdf
15. Handbook of Pharmaceutical Manufacturing, Sarfaraz Niazi.pdf
16. HPLC Methods For Pharmaceutical Analysis, George Lunn.pdf
17. HVAC SYSTEMS TESTING, ADJUSTING & BALANCING.pdf
18. Innovation In Pharmaceutical Industry, Takuji Hara.pdf
19. Introduction to Engineering Statistics and Lean Sigma, Theodore Allen.pdf
20. Introduction to Engineering Statistics and Six Sigma Statistical Quality Control and Design of
Experiments and Systems, Theodore Allen.pdf
21. Introduction to Statistical Quality Control, 5th Edition, Douglas Montgomery.pdf
22. Japanese Pharmacopoeia, 15th Ed.pdf
23. Kualifikasi Kinerja(Performance Qualification) granulasi pengeringan
24. Lean Six Sigma Using sigmaXL and Minitab, Issa Bass.pdf
25. Manufacturing Handbook of Best Practices, Jack Revelle.pdf
26. Mathematical and Statistical Models and Methods in Reliability, Rykov.pdf
27. Meet Minitab 16.pdf
28. Modern Pharmaceutical Industry, Thomas Jacobsen.pdf
29. Open Source Software in Life Science Research, Lee Harland.pdf
30. Paper and Paperboard Packaging Technology, Mark Kirwan.pdf
31. Pharmaceutical and Medical Device Validation by Experimental Design (Informa, 2007), Lynn
Torbeck.pdf
32. Pharmaceutical Dissolution Testing, Jennifer Dressman.pdf
33. Pharmaceutical Manufacturing Encyclopedia (3rd edition)
34. Pharmaceutical Manufacturing Encyclopedia 2nd Edition, Marshall Sittig.pdf
35. Pharmaceutical Manufacturing Encyclopedia 3rd edition, William Andrew.pdf
36. Pharmaceutical Manufacturing Encyclopedia Vol 1 & 2 (2nd Edition 1988) By Marshall Sittig.pdf
37. Pharmaceutical Manufacturing Handbook - Production and processes, Shayne Cox.pdf
38. Pharmaceutical Microbiology, Hugo.pdf
39. Pharmaceutical Packaging Handbook, Edward Bauer.pdf
40. Pharmaceutical Packaging Technology, Dean.pdf
41. Pharmaceutical Process Engineering, Anthony Hickey.pdf
42. Pharmaceutical Production Facilities Design and Aplication.pdf
43. Pharmaceutical Production, Bill Bennett.pdf
44. Pharmaceutical Statistic, Sanford Bolton.pdf
45. Pharmaceutical Statistics Using SAS A Practical Guide SAS Press, Alex Drietmienko.pdf
46. PICS Cleaning Validation.pdf
47. Practical HPLC method development 2ed - Snyder, Kirkland & Glajch.pdf
48. Practical Statistics for the Analytical Scientist, Stephen Ellison.pdf
49. Preformulation in Solid Dosage Form Development. Moji Christianah.pdf
50. Process Capablity Analysis Using Minitab, Keith Bower.pdf
51. Prosedur Penghitungan UCL LCL-Excel2.docx
52. Q2B Validation Of Analytical Procedure, FDA.pdf
53. Good MAnufacturing Practice Guidance For Avtive Pharmaceutical Ingredients, FDA.pdf
54. Quality Control Process Handbook 5th, Juran.pdf
55. Remington_Pharmacy_21th_Ed.iso
56. Review dan Trend Analisis Bahan Baku Produk Bahan Alam 6 April.pdf
57. Rumus perhitungan Cpk.docx
58. Rumus rumus pada Minitab.pdf
59. Semisolid Dosage Forms and Transdermal System.pdf
60. Setting Cleaning Validation Acceptance Limits for Topical, Ovais.pdf
61. Signore dan Jacobs, Good Design Practices for GMP pharmaceutical facilities.pdf
62. Six Sigma in the Pharmaceutical Industry Understanding, Reducing, and Controlling Variation in
Pharmaceuticals and Biologics, Brian K Nunally.pdf
63. Six Sigma Quality Improvement with minitab, Robin Henderson.pdf
64. Solid Dosage Forms and Solid Modified Release Drug Delivery System.pdf
65. Statistical Development of Quality in Medicine Statistics in Practice, Per Winkel.pdf
66. Statistical Method for Assesment of Blend Homogenity, Camilla Medsen.pdf
67. Statistical Methodology in the Pharmaceutical Sciences Statistics a Series of Textbooks and
Monographs, Donald A Berry.pdf
68. Statistical Process Control dan Analisis Kapabilitas Proses.docx
69. Statistical Process Control.pdf
70. Statistics and Chemistry 5th, James N Miller.pdf
71. Statistics and Chemometry 6th edition, James N Miller.pdf
72. Statistics for the Quality Control Chemistry Laboratory, Eamonn Mullins.pdf
73. The Theory and Practice Industrial Pharmacy, Leon Lachman.pdf
74. Total Organic Carbon Calibration Anatel.pdf
75. US Pharmacopeia Method 643 System Suitability Test for Total Organic Carbon
(TOC)Analys.pdf
76. USP Acceptable TOC Levels for Pharmaceutical Shimadzu.pdf
77. USP NF 2009 United States Pharmacopeia 32 National Formulary 27.chm
78. Vaidation and Calibration Of Analytical Instruments, D.Gowrisankar.pdf
79. Validasi Pembersihan.pdf
80. Validated Cleaning Technologies for Pharmaceutical Manufacturing, Destin LeBlanck.pdf
81. Validating Medical Packaging, Ronal Pillchik.pdf
82. Validation and Qualification in Analytical Laboratories, Ludwig Huber.pdf
83. Validation Standard Operating Procedures A Step by Step Guide for Achieving Compliance in
the Pharmaceutical, Medical Device, and Biotech Industries, Second Edition, Syed Imtiaz
Haider.pdf
84. Validation Standard Operating Procedures, Syed Imtiaz Haider.pdf
85. WHO Monographs on Selected Medicinal Plants Volume 1 Who Monographs on Selected
Medicinal Plants.pdf
86. WHO Monographs on Selected Medicinal Plants Volume 2 Who Monographs on Selected
Medicinal Plants.pdf