REFRESHING THE BOOK LINKS-3

1. PHARMACEUTICAL DISPERSE SYSTEMS VOL.1

2. PHARMACEUTICAL DOSAGE FORMS: DISPERSED SYSTEM VOL.2

3. PHARMACEUTICAL DOSAGE FORMS: DISPERSED SYSTEM VOL.3

4.Drug Stability, edited by Carestensen, everything you wnat to know about stability, kinetics, degradation mechanism, ..etc

Drug Stability

5.Generic Development is a good book to R&D personnel, that give clear scheme to develop oral solid product.
Generic Drug product development

6. Coating Technology

7. Analytical Method Development

8. Batch Control System- Design, application and implementation

9. Clinical Drug Trials and Tribulations

10. Dermatological and Transdermal Formulations

12. Stirring theory and practice

13. Handbook of Critical Cleaning_

14. Handbook of Pharmaceutical analysis

16. Pharmaeutical Chemical analysis : Methods for identification and limit tests

17. Pharmaceutical Experimental Design

18. Water Quality Control Handbook

19. Enhancement in drug delivery

20.0 Advanced Pharmaceutical Solids

23.0 Unit Conversion Software

24. Cancer vaccines and tumor vaccines

25. Acute Toxicology Testing

26. Active Pharmaceutical Ingredients

27. The Troubleshooting and maintenance guide for GC

29. WHO monographs on selected medicinal plants

30. Advanced drug formulation design to optimize therapeutic outcomes

31. Analytical Drug Profile vol. 29

32. Analytical method validation and instrument performance verification

33. Antimicrobial Chemotherapy

34.Applied TLC

35. Clean Room Technology

36. Encyclopedia of Medicinal Plants

37. Drug Drug Interactions

38. Drug metabolism in drug design and development

39. Computer application in Pharmaceutical R&D

41. Enhancement in drug delivery

42. FDA Administrative Enforcement Manual

43. GLP Handbook

44. HB of Bioequivalence Testing

45. Int. Biotechnology, Bulk materials and Pharmaceuticals GMPs(Part1)

*** (Part 2)"You shall download 2 parts"

46. GLP Regulations

47. Computer System validation

48. Cosmetics Additives

49. Design of Controlled Release Drug Delivery Systems

50. Development and Validation of HPLC Methods for Analytical and Preparative Purpose

52. Batch Process

53Drug and Controlled Substances Information

54. Injectable Disperse Systems

55. Lippincott Illustrated Pharmacology

56. Stability of drugs and dosage forms

57. Introduction to computational Optimization Models for Production Planning in Supply Chain

59. HVAC Inspection Notes

61. Pharmacology Secrets

62. PVP excipients for pharmaceuticals

63. Traceable temperatures

64. Transport processes in pharmaceuticals

65. Pharmaceutical Dissolution Testing

66. Sterile Filtration

67. Encyclopedia of Controlled Drug Delivery Part I

68.Encyclopedia of Controlled Drug Delivery Part II

69. Handbook of Pharmaceutical Excipients

70.Drug Safety Evaluation

71. Compliance Handbook for pharmaceuticals, Medical Device and Biologics

72. Encyclopedia of Pharmaceutical Technology

74. Effective Drug Regulations

76. Clinical Trial Risk Managment

77. Fundamnetals of Environmental Sampling and analysis

78. Vogel's Textbook of Quantitative Chemical Analysis

79. Understanding Mass Spectra

80. Pharmaceutical Regulatory Process

81. Waste Water Quality Monitor and Treatment

82. Validation and Qualification of Analytical Laboratories

83. Validating Chromatographic Methods

84. Water Insoluble Drug Formulations

85. Analytcal Profile of Drug substances volume 33

86. Spectroscoy of Pharmaceutical Solids

87. Statistics in Drug Research

88. A Century of Separation Science

89. Free Energy Calculations in Rational Drug Design

90. Facility Management Handbook

91. Filtration and Purification in the Biopharmaceutical Industry

92. Drug Delivery Systems

94. Facility Validation

95. Electronic Record Keeping

96. Excipient Development for Pharmaceutical Biotechnology and Drug Delivery Systems

97. Fundamentals of HVAC Systems

98. Drug Facts and Comparisons

99. Carbon C13 NMR Spectroscopy

100. Aqueous Cleaning Handbook