The document discusses Good Laboratory Practices (GLP) for pharmaceutical quality control laboratories. It covers GLP requirements from regulatory authorities like the FDA and WHO. The presentation is divided into sections on lab management, resource management, and quality control activities. Lab management covers topics like laboratory entry and exit procedures, safety, and upkeep. Resource management addresses management of personnel, procedures, reagents, instruments, and documentation. Quality control activities include sampling, chromatography, microbiology, stability testing, and documentation of investigations. Maintaining GLP standards helps ensure quality products for patients and regulatory compliance.

1. GOOD LABORATORY
PRACTICES
Presented By:
ABDULLA HEL KAFEE
Date : 19.09.2021

2. The IBN SINA Pharmaceutical Industry Ltd. is
committed to–
Serve humanity by manufacturing and providing quality medicines and
services to it’s customers ;
Maintaining the ethical standard in all it’s functions following the
requirements of cGMP and regulatory authorities ;
 Marching onward for sustainable growth and continual improvement.

3. Introduction

4. Introduction ( Continue..)

5. Requirements of GLP
( 21 CFR Part 211, Subpart I- Laboratory Controls )

6. Requirements of GLP
( WHO Good practices for pharmaceutical quality control laboratories )

7. Requirements of GLP
( ISO/IEC 17025)

8. Activity wise GLP in QC

9. Lab Management
Laboratory Entry

10. Lab Management
Laboratory Entry ( Continue…)

11. Lab Management
Laboratory Exit

12. Lab Management
Laboratory Safety

13. Lab Management
Laboratory Safety (Continue…)

14. Lab Management
Laboratory Safety (Continue…)

15. Lab Management
Laboratory Safety (Continue…)

16. Lab Management
Laboratory Safety (Continue…)

17. Lab Management
Laboratory Safety (Continue…)

18. Lab Management
Laboratory Upkeep

19. Lab Management
Laboratory Upkeep (Continue…)

20. Lab Management
Laboratory Upkeep (Continue…)

21. Lab Management
Laboratory Upkeep (Continue…)

22. Lab Management
Laboratory Upkeep (Continue…)

23. Lab Management
Laboratory Upkeep (Continue…)

24. Lab Management
Laboratory Upkeep (Continue…)

25. Lab Management
Laboratory Upkeep (Continue…)

26. Lab Management
Laboratory Behavior

27. Resource Management
People

28. Resource Management
Procedures

29. Resource Management
Procedures (Continue…)

30. Resource Management
Procedures (Continue…)

31. Resource Management
Procedures (Continue…)

32. Resource Management
Reagents , Chemicals & Solvents

33. Resource Management
Reagents , Chemicals & Solvents
(Continue…)

34. Resource Management
Standards

35. Resource Management
Standards (Continue…)

36. Resource Management
Glassware

37. Resource Management
Instruments

38. Resource Management
Instruments (Continue…)

39. Resource Management
Instruments (Continue…)

40. Resource Management
Log Books

41. Resource Management
Log Books ( Continue…)

42. Resource Management
Computers

43. QC Activities
Sampling

44. QC Activities
Sampling(Continue…)

45. QC Activities
Weighing

46. QC Activities
Measuring Volume

47. QC Activities
Measuring Volume(Continue…)

48. QC Activities
Sample Preparation

49. QC Activities
Sample Preparation(Continue…)

50. QC Activities
Chromatography

51. QC Activities
Chromatography (Continue…)

52. QC Activities
Chromatography (Continue…)

53. QC Activities
Chromatography (Continue…)

54. QC Activities
Microbiology

55. QC Activities
Microbiology (Continue…)

56. QC Activities
Microbiology (Continue…)

57. QC Activities
Microbiology (Continue…)

58. QC Activities
Stability

59. QC Activities
Stability (Continue…)

60. QC Activities
Stability (Continue…)

61. QC Activities
Documentation

62. QC Activities
Documentation(Continue…)

63. QC Activities
Documentation(Continue…)

64. QC Activities
Documentation(Continue…)

65. QC Activities
Investigations

66. QC Activities
Investigations(Continue…)

67. QC Activities
Investigations(Continue…)

68. QC Activities
Investigations(Continue…)

69. Thank You
Thank you for attending this training course.
By keeping the data quality attributes (ALCOA) in the forefront of our minds,
we can:
Supply safe and effective products to our patients and consumers
Maintain compliance so that we can .
Keep in mind that the customers and patients relies on us and
the accuracy of our data!