Laboratory auditing for quality and regulatory compliance

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Hauptverfasser: Singer, Donald C. (VerfasserIn), Stefan, Raluca-Ioana (VerfasserIn), Van Staden, Jacobus Frederick (VerfasserIn)
Format: Buch
Sprache:English
Veröffentlicht: Boca Raton, Fla. Taylor&Francis 2005
Schriftenreihe:Drugs and the pharmaceutical sciences 150
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Datensatz im Suchindex

_version_ 1819764061960667136
adam_text DRUGS AND THE PHARMACEUTICAL SCIENCES A Series of Textbooks and Monographs 1. Pharmacokinetics, Milo Gibaldi and Donald Perrier 2. Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control, Sidney H. Willig, Murray M. Tuckerman, and William S. Hitchings IV 3. Microencapsulation, edited by J. R. Nixon 4. Drug Metabolism: Chemical and Biochemical Aspects, Bernard Testa and Peter Jenner 5. New Drugs: Discovery and Development, edited by Alan A. Rubin 6. Sustained and Controlled Release Drug Delivery Systems, edited by Joseph R. Robinson 7. Modern Pharmaceutics, edited by Gilbert S. Banker and Christopher T. Rhodes 8. Prescription Drugs in Short Supply: Case Histories, Michael A. Schwartz 9. Activated Charcoal: Antidotal and Other Medical Uses, David O. Cooney 10. Concepts in Drug Metabolism (in two parts), edited by Peter Jenner and Bernard Testa 11. Pharmaceutical Analysis: Modern Methods (in two parts), edited by James W. Munson 12. Techniques of Solubilization of Drugs, edited by Samuel H. Yalkowsky 13. Orphan Drugs, edited by Fred E. Karch 14. Novel Drug Delivery Systems: Fundamentals, Developmental Concepts, Biomedical Assessments, Yie W. Chien 15. Pharmacokinetics: Second Edition, Revised and Expanded, Milo Gibaldi and Donald Perrier 16. Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control, Second Edition, Revised and Expanded, Sidney H. Willig, Murray M. Tuckerman, and William S. Hitchings IV 17. Formulation of Veterinary Dosage Forms, edited by Jack Blodinger 18. Dermatological Formulations: Percutaneous Absorption, Brian W. Barry 19. The Clinical Research Process in the Pharmaceutical Industry, edited by Gary M. Matoren 20. Microencapsulation and Related Drug Processes, Patrick B. Deasy 21. Drugs and Nutrients: The Interactive Effects, edited by Daphne A. Roe and T. Colin Campbell 22. Biotechnology of Industrial Antibiotics, Erick J. Vandamme 23. Pharmaceutical Process Validation, edited by Bernard T. Loftus and Robert A. Nash 24. Anticancer and Interferon Agents: Synthesis and Properties, edited by Raphael M. Ottenbrite and George B. Butler 25. Pharmaceutical Statistics: Practical and Clinical Applications, Sanford Bolton 26. Drug Dynamics for Analytical, Clinical, and Biological Chemists, Benjamin J. Gudzinowicz, Burrows T. Younkin, Jr., and Michael J. Gudzinowicz 27. Modern Analysis of Antibiotics, edited by Adjoran Aszalos 28. Solubility and Related Properties, Kenneth C. James 29. Controlled Drug Delivery: Fundamentals and Applications, Second Edition, Revised and Expanded, edited by Joseph Ft. Robinson and Vincent H. Lee 30. New Drug Approval Process: Clinical and Regulatory Management, edited by Richard A. Guarino 31. Transdermal Controlled Systemic Medications, edited by Vie W. Chien 32. Drug Delivery Devices: Fundamentals and Applications, edited by Praveen Tyle 33. Pharmacokinetics: Regulatory • Industrial • Academic Perspectives, edited by Peter G. Welling and Francis L S. Tse 34. Clinical Drug Trials and Tribulations, edited by Allen E. Cato 35. Transdermal Drug Delivery: Developmental Issues and Research Initiatives, edited by Jonathan Hadgraft and Richard H. Guy 36. Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms, edited by James W. McGinity 37. Pharmaceutical Pelletization Technology, edited by Isaac Ghebre Sellassie 38. Good Laboratory Practice Regulations, edited by Allen F. Hirsch 39. Nasal Systemic Drug Delivery, Vie W. Chien, Kenneth S. E. Su, and Shyi Feu Chang 40. Modern Pharmaceutics: Second Edition, Revised and Expanded, edited by Gilbert S. Banker and Christopher T. Rhodes 41. Specialized Drug Delivery Systems: Manufacturing and Production Technology, edited by Praveen Tyle 42. Topical Drug Delivery Formulations, edited by David W. Osborne and Anton H. Amann 43. Drug Stability: Principles and Practices, Jens T, Carstensen 44. Pharmaceutical Statistics: Practical and Clinical Applications, Second Edition, Revised and Expanded, Sanford Bolton 45. Biodegradable Polymers as Drug Delivery Systems, edited by Mark Chasin and Robert Langer 46. Preclinical Drug Disposition: A Laboratory Handbook, Francis L S. Tse and James J. Jaffe 47. HPLC in the Pharmaceutical Industry, edited by Godwin W. Fong and Stanley K. Lam 48. Pharmaceutical Bioequivalence, edited by Peter G. Welling, Francis L. S. Tse, and Shrikant V. Dinghe 49. Pharmaceutical Dissolution Testing, Umesh V. Banakar 50. Novel Drug Delivery Systems: Second Edition, Revised and Expanded, Yie W. Chien 51. Managing the Clinical Drug Development Process, David M. Cocchetto and Ronald V. Nardi 52. Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control, Third Edition, edited by Sidney H. Willig and James R. Stoker 53. Prodrugs: Topical and Ocular Drug Delivery, edited by Kenneth B. Sloan 54. Pharmaceutical Inhalation Aerosol Technology, edited by Anthony J. Hickey 55. Radiopharmaceuticals: Chemistry and Pharmacology, edited by Adrian D. Nunn 56. New Drug Approval Process: Second Edition, Revised and Expanded, edited by Richard A. Guarino 57. Pharmaceutical Process Validation: Second Edition, Revised and Expanded, edited by Ira R. Berry and Robert A. Nash 58. Ophthalmic Drug Delivery Systems, edited by Ashim K. Mitra 59. Pharmaceutical Skin Penetration Enhancement, edited by Kenneth A. Walters and Jonathan Hadgraft 60. Colonic Drug Absorption and Metabolism, edited by Peter R. Bieck 61. Pharmaceutical Particulate Carriers: Therapeutic Applications, edited by Alain Rolland 62. Drug Permeation Enhancement: Theory and Applications, edited by Dean S. Hsieh 63. Glycopeptide Antibiotics, edited by Ramakrishnan Nagarajan 64. Achieving Sterility in Medical and Pharmaceutical Products, Nigel A. Halls 65. Multiparticulate Oral Drug Delivery, edited by Isaac Ghebre Sellassie 66. Colloidal Drug Delivery Systems, edited by Jorg Kreuter 67. Pharmacokinetics: Regulatory • Industrial • Academic Perspectives, Second Edition, edited by Peter G. Welling and Francis L S. Tse 68. Drug Stability: Principles and Practices, Second Edition, Revised and Expanded, Jens T. Carstensen 69. Good Laboratory Practice Regulations: Second Edition, Revised and Expanded, edited by Sandy Weinberg 70. Physical Characterization of Pharmaceutical Solids, edited by Harry G. Brittain 71. Pharmaceutical Powder Compaction Technology, edited by Goran Alderborn and Christer Nystrom 72. Modern Pharmaceutics: Third Edition, Revised and Expanded, edited by Gilbert S. Banker and Christopher T. Rhodes 73. Microencapsulation: Methods and Industrial Applications, edited by Simon Benita 74. Oral Mucosal Drug Delivery, edited by Michael J. Rathbone 75. Clinical Research in Pharmaceutical Development, edited by Barry Bleidt and Michael Montagne 76. The Drug Development Process: Increasing Efficiency and Cost Effectiveness, edited by Peter G. Welling, Louis Lasagna, and Umesh V. Banakar 77. Microparticulate Systems for the Delivery of Proteins and Vaccines, edited by Smadar Cohen and Howard Bernstein 78. Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control, Fourth Edition, Revised and Expanded, Sidney H. Willig and James R. Stoker 79. Aqueous Polymeric Coatings for Pharmaceutical Dosage Forms: Second Edition, Revised and Expanded, edited by James W. McGinity 80. Pharmaceutical Statistics: Practical and Clinical Applications, Third Edition, Sanford Bolton 81. Handbook of Pharmaceutical Granulation Technology, edited by Dilip M. Parikh 82. Biotechnology of Antibiotics: Second Edition, Revised and Expanded, edited by William R. Strohl 83. Mechanisms of Transdermal Drug Delivery, edited by Russell O. Potts and Richard H. Guy 84. Pharmaceutical Enzymes, edited by Albert Lauwers and Simon Scharpe 85. Development of Biopharmaceutical Parenteral Dosage Forms, edited by John A. Bontempo 86. Pharmaceutical Project Management, edited by Tony Kennedy 87. Drug Products for Clinical Trials: An International Guide to Formulation • Production • Quality Control, edited by Donald C. Monkhouse and Christopher T. Rhodes 88. Development and Formulation of Veterinary Dosage Forms: Second Edition, Revised and Expanded, edited by Gregory £ Hardee and J. Desmond Baggot 89. Receptor Based Drug Design, edited by Paul Left 90. Automation and Validation of Information in Pharmaceutical Processing, edited by Joseph F. deSpautz 91. Dermal Absorption and Toxicity Assessment, edited by Michael S. Roberts and Kenneth A. Walters 92. Pharmaceutical Experimental Design, Gareth A. Lewis, Didier Mathieu, and Roger Phan Tan Luu 93. Preparing for FDA Pre Approval Inspections, edited by Martin D. Hynes III 94. Pharmaceutical Excipients: Characterization by IR, Raman, and NMR Spectroscopy, David E. Bugay and W. Paul Findlay 95. Polymorphism in Pharmaceutical Solids, edited by Harry G. Brittain 96. Freeze Drying/Lyophilization of Pharmaceutical and Biological Products, edited by Louis Rey and Joan C. May 97. Percutaneous Absorption: Drugs Cosmetics Mechanisms Methodology, Third Edition, Revised and Expanded, edited by Robert L. Bronaugh and Howard I. Maibach 98. Bioadhesive Drug Delivery Systems: Fundamentals, Novel Approaches, and Development, edited by Edith Mathiowitz, Donald E. Chickering III, and Claus Michael Lehr 99. Protein Formulation and Delivery, edited by Eugene J. McNally 100. New Drug Approval Process: Third Edition, The Global Challenge, edited by Richard A. Guarino 101. Peptide and Protein Drug Analysis, edited by Ronald E. Reid 102. Transport Processes in Pharmaceutical Systems, edited by Gordon L. Amidon, Ping I. Lee, and Elizabeth M. Topp 103. Excipient Toxicity and Safety, edited by Myra L. Weiner and Lois A. Kotkoskie 104. The Clinical Audit in Pharmaceutical Development, edited by Michael R. Hamrell 105. Pharmaceutical Emulsions and Suspensions, edited by Francoise Nielloud and Gilberte Marti Mestres 106. Oral Drug Absorption: Prediction and Assessment, edited by Jennifer B. Dressman and Hans Lennernas 107. Drug Stability: Principles and Practices, Third Edition, Revised and Expanded, edited by Jens T. Carstensen and C. T. Rhodes 108. Containment in the Pharmaceutical Industry, edited by James P. Wood 109. Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control from Manufacturer to Consumer, Fifth Edition, Revised and Expanded, Sidney H. Willig 110. Advanced Pharmaceutical Solids, Jens T. Carstensen 111. Endotoxins: Pyrogens, LAL Testing, and Depyrogenation, Second Edition, Revised and Expanded, Kevin L. Williams 112. Pharmaceutical Process Engineering, Anthony J. Hickey and David Ganderton 113. Pharmacogenomics, edited by Werner Kalow, Urs A. Meyer, and Rachel F. Tyndale 114. Handbook of Drug Screening, edited by Ramakrishna Seethala and Prabhavathi B. Fernandes 115. Drug Targeting Technology: Physical • Chemical • Biological Methods, edited by Hans Schreier 116. Drug Drug Interactions, edited by A. David Rodrigues 117. Handbook of Pharmaceutical Analysis, edited by Lena Ohannesian and Anthony J. Streeter 118. Pharmaceutical Process Scale Up, edited by Michael Levin 119. Dermatological and Transdermal Formulations, edited by Kenneth A. Walters 120. Clinical Drug Trials and Tribulations: Second Edition, Revised and Expanded, edited by Allen Cato, Lynda Sutton, and Allen Cato III 121. Modern Pharmaceutics: Fourth Edition, Revised and Expanded, edited by Gilbert S. Banker and Christopher T. Rhodes 122. Surfactants and Polymers in Drug Delivery, Martin Malmsten 123. Transdermal Drug Delivery: Second Edition, Revised and Expanded, edited by Richard H. Guy and Jonathan Hadgraft 124. Good Laboratory Practice Regulations: Second Edition, Revised and Expanded, edited by Sandy Weinberg 125. Parenteral Quality Control: Sterility, Pyrogen, Particulate, and Package Integrity Testing: Third Edition, Revised and Expanded, Michael J. Akers, Daniel S. Larrimore, and Dana Morton Guazzo 126. Modified Release Drug Delivery Technology, edited by Michael J. Rathbone, Jonathan Hadgraft, and Michael S. Roberts 127. Simulation for Designing Clinical Trials: A Pharmacokinetic Pharmacodynamic Modeling Perspective, edited by Hui C. Kimko and Stephen B. Duffull 128. Affinity Capillary Electrophoresis in Pharmaceutics and Biopharmaceutics, edited by Reinhard H. H. Neubert and Hans Hermann Ruttinger 129. Pharmaceutical Process Validation: An International Third Edition, Revised and Expanded, edited by Robert A. Nash and Alfred H. Wachter 130. Ophthalmic Drug Delivery Systems: Second Edition, Revised and Expanded, edited by Ashim K. Mitra 131. Pharmaceutical Gene Delivery Systems, edited by Alain Rolland and Sean M. Sullivan 132. Biomarkers in Clinical Drug Development, edited by John C. Bloom and Robert A. Dean 133. Pharmaceutical Extrusion Technology, edited by Isaac Ghebre Sellassie and Charles Martin 134. Pharmaceutical Inhalation Aerosol Technology: Second Edition, Revised and Expanded, edited by Anthony J. Hickey 135. Pharmaceutical Statistics: Practical and Clinical Applications, Fourth Edition, Sanford Bolton and Charles Bon 136. Compliance Handbook for Pharmaceuticals, Medical Devices, I and Biologies, edited by Carmen Medina j 137. Freeze Drying/Lyophilization of Pharmaceutical and Biological Products: Second Edition, Revised and Expanded, edited by Louis Rey and Joan C, May 138. Supercritical Fluid Technology for Drug Product Development, edited by Peter York, Uday B. Kompella, and Boris Y Shekunov 139. New Drug Approval Process: Fourth Edition, Accelerating Global Registrations, edited by Richard A. Guarino 140. Microbial Contamination Control in Parenteral Manufacturing, edited by Kevin L Williams 141. New Drug Development: Regulatory Paradigms for Clinical Pharmacology and Biopharmaceutics, edited by Chandrahas G. Sahajwalla 142. Microbial Contamination Control in the Pharmaceutical Industry, edited by Luis Jimenez 143. Generic Drug Product Development: Solid Oral Dosage Forms, edited by Leon Shargel and Izzy Kanfer 144. Introduction to the Pharmaceutical Regulatory Process, edited by Ira R. Berry 145. Drug Delivery to the Oral Cavity: Molecules to Market, edited by Tapash K. Ghosh and William R. Pfister 146. Good Design Practices for GMP Pharmaceutical Facilities, edited by Andrew Signore and Terry Jacobs 147. Drug Products for Clinical Trials, Second Edition, edited by Donald Monkhouse, Charles Carney, and Jim Clark 148. Polymeric Drug Delivery Systems, edited by Glen S. Kwon 149. Injectable Dispersed Systems: Formulation, Processing, and Performance, edited by Diane J. Burgess 150. Laboratory Auditing for Quality and Regulatory Compliance, Donald C. Singer, Raluca loana Stefan, and Jacobus F. van Staden CONTENTS Preface .... Hi Introduction .... vii I. Quality and Auditing / Quality Control and Quality Assurance in a Laboratory .... 1 The Regulated Industries .... 3 Goals of a Laboratory Quality Audit .... 5 Audit Tools: Observation, Working Knowledge, and Audit Documents .... 7 II. Nontechnical Parameters for Evaluation 9 Quality Programs, Documentation, and Organizational Structure .... 9 Personnel .... 14 Facility and Environment .... 15 III. Technical Parameters for Evaluation 19 Sample Control .... 19 Instrumentation .... 20 Automation of Analytical Process .... 22 Acquisition and Processing of Data .... 23 Uncertainty of Measurements .... 24 Reliability of Measurements .... 26 Standards and Standardization .... 26 Supplies Organization .... 27 Proficiency Testing .... 28 v Vi Contents IV. Other Areas to Consider 29 Customer Satisfaction .... 29 Laboratory Health and Safety .... 29 V. Communications and Follow Up 31 Closing Conference, Final Report, and Follow Up .... 31 Frequency of Audit .... 33 Epilog 35 Appendices A. Sample Laboratory Quality Audit Document .... 37 B. National Voluntary Laboratory Accreditation Program, NIST Handbook 150 .... 51 C. Guide to Quality in Analytical Chemistry (Eurachem/CITAC) .... 117 D. Quality Assurance for Research and Development and Nonroutine Analysis (EURACHEM/CITAC) .... 175 E. Accreditation for Microbiological Laboratories (Eurachem/EA) .... 229 F. EPA Manual for Certification of Laboratories Analyzing Drinking Water .... 253 G. Federal Register (FDA): Good Laboratory Practice Regulations for Nonclinical Laboratory Studies .... 443 Bibliography 465 Index 469
any_adam_object 1
author Singer, Donald C.
Stefan, Raluca-Ioana
Van Staden, Jacobus Frederick
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Stefan, Raluca-Ioana
Van Staden, Jacobus Frederick
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author_sort Singer, Donald C.
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r i s ris
s j f v sjf sjfv
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dewey-hundreds 300 - Social sciences
dewey-ones 362 - Social problems and services to groups
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dewey-tens 360 - Social problems and services; associations
discipline Soziologie
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id DE-604.BV020049872
illustrated Illustrated
indexdate 2024-12-23T18:22:38Z
institution BVB
isbn 1574445707
language English
lccn 2005043739
oai_aleph_id oai:aleph.bib-bvb.de:BVB01-013370824
oclc_num 58790971
open_access_boolean
owner DE-12
owner_facet DE-12
physical VIII, 471 S. Ill.
publishDate 2005
publishDateSearch 2005
publishDateSort 2005
publisher Taylor&Francis
record_format marc
series Drugs and the pharmaceutical sciences
series2 Drugs and the pharmaceutical sciences
spellingShingle Singer, Donald C.
Stefan, Raluca-Ioana
Van Staden, Jacobus Frederick
Laboratory auditing for quality and regulatory compliance
Drugs and the pharmaceutical sciences
Laboratoires - Qualité - Contrôle
Médecine - Laboratoires - Qualité - Contrôle
Medical laboratories Quality control
Laboratories Quality control
Forschung (DE-588)4017894-8 gnd
Pharmazie (DE-588)4045705-9 gnd
Medizinisches Labor (DE-588)4193766-1 gnd
Laboratorium (DE-588)4033927-0 gnd
Pharmazeutische Industrie (DE-588)4045696-1 gnd
Qualitätssicherung (DE-588)4126457-5 gnd
subject_GND (DE-588)4017894-8
(DE-588)4045705-9
(DE-588)4193766-1
(DE-588)4033927-0
(DE-588)4045696-1
(DE-588)4126457-5
title Laboratory auditing for quality and regulatory compliance
title_auth Laboratory auditing for quality and regulatory compliance
title_exact_search Laboratory auditing for quality and regulatory compliance
title_full Laboratory auditing for quality and regulatory compliance Donald C. Singer , Raluca-Joana Stefan, Jacobus F. van Staden
title_fullStr Laboratory auditing for quality and regulatory compliance Donald C. Singer , Raluca-Joana Stefan, Jacobus F. van Staden
title_full_unstemmed Laboratory auditing for quality and regulatory compliance Donald C. Singer , Raluca-Joana Stefan, Jacobus F. van Staden
title_short Laboratory auditing for quality and regulatory compliance
title_sort laboratory auditing for quality and regulatory compliance
topic Laboratoires - Qualité - Contrôle
Médecine - Laboratoires - Qualité - Contrôle
Medical laboratories Quality control
Laboratories Quality control
Forschung (DE-588)4017894-8 gnd
Pharmazie (DE-588)4045705-9 gnd
Medizinisches Labor (DE-588)4193766-1 gnd
Laboratorium (DE-588)4033927-0 gnd
Pharmazeutische Industrie (DE-588)4045696-1 gnd
Qualitätssicherung (DE-588)4126457-5 gnd
topic_facet Laboratoires - Qualité - Contrôle
Médecine - Laboratoires - Qualité - Contrôle
Medical laboratories Quality control
Laboratories Quality control
Forschung
Pharmazie
Medizinisches Labor
Laboratorium
Pharmazeutische Industrie
Qualitätssicherung
url http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=013370824&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
volume_link (DE-604)BV000002008
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AT stefanralucaioana laboratoryauditingforqualityandregulatorycompliance
AT vanstadenjacobusfrederick laboratoryauditingforqualityandregulatorycompliance