Quality Control in Clinical Chemistry
eBook - PDF

Quality Control in Clinical Chemistry

  1. 578 pages
  2. English
  3. PDF
  4. Available on iOS & Android
eBook - PDF

Quality Control in Clinical Chemistry

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Yes, you can access Quality Control in Clinical Chemistry by Guillermo A. Anido, S. B. Rosalki, E. J. van Kampen, M. Rubin in PDF and/or ePUB format, as well as other popular books in Medicine & Internal Medicine & Diagnosis. We have over one million books available in our catalogue for you to explore.

Information

Publisher
De Gruyter
Year
2014
Print ISBN
9783110066920
eBook ISBN
9783110846478

Table of contents

  1. Foreword
  2. Opening Session: Welcome by the Chairman
  3. Introduction
  4. Award Lectures: Topic I: Quality Control in Relation to Determination Methods
  5. Considerations on Bilirubin Determination
  6. Comparison between Determination Methods
  7. Interlaboratory Quality Control using the Daily Means of Patients Results
  8. Discussion: Topic II: Quality Control in Relation to Determination Materials, Standards and Controls
  9. Evaluation of some Determination Materials used in the Scandinavian Recommended Methods (S.C.E.) for Determination of Four Enzymes in Blood and the Performance of Control Materials with these Methods
  10. The Control of Error and Use of Standardized Reference Samples in Estimation of the True Biological Normal Range
  11. Studies on Alkaline Phosphatases of Different Origin with an External Quality Control Scheme
  12. Evaluation of Several Commercial Controls.Correlation between them
  13. Interlaboratory Comparison of both Accuracy and Precision by a Two-Sample Method
  14. The World Health Organization-Center for Disease Control Lipid Standardization Program
  15. Discussion: Topic III: Quality Control in Relation to Data Evaluation, Processing and Presentation
  16. The Determination of Assigned Values for Control Specimens
  17. The Role of External Quality Control Schemes in Improving the Quality of Laboratory Results
  18. Computerized Techniques for Quality Control in the Clinical Chemistry Laboratory
  19. Systems Analysis of Analytical Procedures as a Means of Improving their Performance
  20. Discussion of the Options Followed in Processing Quality Control Data
  21. Discussion: Richterich Memorial Lecture
  22. Introduction
  23. Seeking the way
  24. NAD - NADH - NADP - NADPH Characterization and Purity Assurance Plenary Lectures
  25. Quality Requirements for ß-NADH and ß-NAD
  26. Studies on the Purity and Storage of NADH
  27. Free Communications
  28. The Molar Absorption Coefficient (e) of Reduced NAD (NADH)
  29. The Molar Absorption Coefficients of ß-Nicotinamide-Adenine Dinucleotide
  30. Stability of NADH Containing Reagent for the Determination of Transaminases on the Greiner Selective Analyzer GSA II
  31. The Contribution of Spectrophotometric Instrument Month to Month Variability to the Precision of Molar Concentration Measurements using the Molar Absorptivity Constant for NADH: Two Years of Spectrophotometric Precision Monitoring using United States National Bureau of Standards Absorbance Standards at 3 Absorbance Levels
  32. NAD Quality Control: Standardization of Methods for the Selection of an NAD Coenzyme
  33. A Convenient Enzyme System for the Evaluation of NADH Preparations
  34. Clinical Studies of a System for the Evaluation of NADH Purity: Part I
  35. Clinical Studies of a System for the Evaluation of NADH Purity: Part II
  36. Comparison of Mammalian Tissue Extracts and Evaluation of a System for the Detection of Enzyme Inhibitors in NADH Preparations
  37. Temperature Dependence of Difference-Absorption Coefficients of NADH Minus NAD+ and NADPH Minus NADP+ in the near Ultraviolet
  38. Discussion: Hematology Symposium Plenary Lectures
  39. Quality Control and Hematology I
  40. Quality Control and Hematology II
  41. Discussion:A First Transatlantic, Live Demonstration of a Computerized Audio-Response Communications System of an Automated Clinical Laboratory
  42. The First International Symposium on Quality Control, Tokyo
  43. Chairman’s Closing Remarks
  44. Award Presentations
  45. International Federation of Clinical Chemistry The Clinical Laboratory from an International Viewpoint Session I: Topic: International Criteria for Clinical Laboratory Materials
  46. International Criteria for Reference Materials
  47. International Criteria for Diagnostic Material
  48. Acceptability of Quality Control Materials
  49. A System Approach to Calibration and Quality Control Materials
  50. Discussion: Session II: Topic: International Criteria for Diagnostic Methods
  51. Acceptability of Definitive, Reference and Routine Methods
  52. Acceptability of Simplified Methods
  53. The Development of Simplified Tests
  54. The Acceptability of Enzyme Methods
  55. Acceptability of Diagnostic Kits
  56. Materials and Methods for Health Testing
  57. Discussion: Session III: Topic: International Criteria for Clinical Laboratory Instrumentation
  58. Opening Remarks
  59. National Committee for Clinical Laboratory Standards a Model for Achieving International Clinical Laboratory Consensus Standards
  60. International Requirements for Instrumentation in Clinical Chemistry
  61. International Criteria for Determining the Acceptability of Laboratory Instrumentation
  62. Discussion: Session IV: Topic: National Regulations and International Recommendations
  63. The Regulation of Diagnostic Products in the United States
  64. Analysis of Regulations on Clinical Chemistry in the European Community
  65. National Regulations and International Recommendations in Laboratory Diagnosis in Socialistic Countries
  66. Discussion and Closing Remarks
  67. Speakers List