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Cleaning Validation : Practical Compliance Approaches for Pharmaceutical Manufacturing

Cleaning Validation : Practical Compliance Approaches for Pharmaceutical Manufacturing (Paperback)

Destin A. Leblanc (지은이)
CRC Press
66,800원

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Cleaning Validation : Practical Compliance Approaches for Pharmaceutical Manufacturing
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책 정보

· 제목 : Cleaning Validation : Practical Compliance Approaches for Pharmaceutical Manufacturing (Paperback) 
· 분류 : 외국도서 > 의학 > 전염병학
· ISBN : 9781032431734
· 쪽수 : 216쪽
· 출판일 : 2024-10-09

목차

          Terminology

  1. Use of the Term "Product"
  2. Use of the Terms Grouping and Matrixing
  3. Deviations and Nonconformances
  4. Clarifying Terms: Blanks vs. Controls
  5. Meaning of "Dedicated"?
  6. Words (Again??)
  7. Health-based Limits

  8. What's at Stake with HBELs
  9. A Look at the Revised Risk-MaPP
  10. EMA's Q&A Clarification: Part 1
  11. EMA's Q&A Clarification: Part 2
  12. The EMA Q&A "Clarification" on Limits
  13. The EMA Q&A on Routine Analytical Testing
  14. Other Issues in EMA's Q&A
  15. Highly Hazardous Products in Shared Facilities
  16.  Limits - General

  17. EMA vs. ISPE on Cleaning Limits?
  18. Does a High "Margin of Safety" Protect Patients?
  19. What If the Next Product is the Same Product?
  20. Limits for "Product A to Product A"
  21. Surfaces Areas in Carryover Calculations
  22. Carryover Calculation Errors to Avoid
  23. Protocol Limits for Yeasts/Molds?
  24. Cleaning Validation for Homeopathic Drug Products
  25. A Possible Approach for Biotech Limits
  26. Establishing Clearance for Degraded Protein Actives
  27.  Visually Clean

  28. Avoiding "Visually Dirty" Observations
  29. What's a Visual Limit?
  30. Visual Residue Limits ? Part 1
  31. Visual Residue Limits ? Part 2
  32. Analytical and Sampling Methods

  33. Two More Nails in the Coffin?
  34. More Swab Sampling Issues
  35. Timing for Swab Sampling in a Protocol?
  36. Pass/Fail Analytical Test Methods
     
  37. Product Grouping

  38. Issues in Product Grouping
  39. Toxicity as a Worst-Case Grouping Factor
  40. Another "Worst Case" Product Grouping Idea
     
  41. Protocols and Procedures

  42. Issues in Rinsing - Part 1
  43. Issues in Rinsing - Part 2
  44. Routine Monitoring for Highly Hazardous Products
  45. "Concurrent Release" for Cleaning Validation
  46. Dirty and Clean Hold Time Protocols
  47. API Manufacture

  48. A Critique of the APIC Guideline
  49. Another Issue for API Synthesis
  50. Contaminants in API Manufacture
     
  51. Miscellaneous

  52. Significant Figures: Back to Basics
  53. The Value of a Protocol Worksheet for Manual Cleaning
  54. Dealing with Used and New Equipment
  55. Solving Cleaning Validation Problems by Analogy
  56. Causing Cleaning Validation Problems by Analogy

 

Appendix A: Acronyms Used in this Volume

Appendix B: Shorthand Notations for Expressing Limits

Index

저자소개

Destin A. Leblanc (지은이)    정보 더보기
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