GLP

1. Good (Safe) Laboratory Practices for Pharmaceuticals
2. Understanding the Difference Between Standardization and Verification of Analytical Methods in Medicine
3. HPLC System Software Validation Plan Steps for HPLC Method Validation
4. Why is Analytical Method Validation Required?
5. Importance of Data Integrity in Pharmaceuticals
6. FDA New Data Integrity Guidelines: Highlights
7. Importance of Microbiological Analysis in Cleaning Method Validation
8. Steps for HPLC Method Development
9. Steps for Analytical Method Development
10. Relative Response Factor (RRF) and its Calculation in HPLC Analysis
11. Data Integrity in Microbial Analysis
12. Event Tree Analysis (ETA) in Pharmaceuticals
13. Data Integrity as per 21 CFR Rules
14. Insight on Data Integrity in Chromatography
15. 6 Ways to Reduce Human Errors in Pharmaceuticals
16. Concept of GxP in Pharmaceuticals
17. Planning and Execution of Internal Audits in Pharmaceuticals
18. Components of GMP: GMP in Detail
19. Working Principle of pH Meter
20. Impact of Culture and Behaviors on Data Integrity Compliance in Pharmaceuticals
21. Best Practices for Isolator Technology
22. Tips for Hazardous Chemical Handling in Laboratory
23. Limitations and Advances in Dissolution Testing in Pharmaceuticals
24. The Role of 21 CFR Part 11 in the Laboratory
25. Best Practices in Microbiology Laboratory in Pharmaceuticals
26. Extraneous Peaks in Chromatographic Analysis
27. Data Integrity Survey Results
28. Build a Quality Culture in Pharmaceuticals
29. Biosimilars and their Significance in Pharmaceuticals
30. Determination of Hot and Cold Spot in Stability Chamber
31. What does Inspector Look for during FDA Inspection?
32. Analytical Balances Drift and Its Importance
33. Audit Trail Requirements in Pharmaceuticals
34. pH Value, pH Scale and Its Measurement between 0 and 14
35. SOP for Good Laboratory Practice (GLP)
36. GLP in Microbiology Laboratory
37. Environmental Isolates and Their Library in Sterile Pharmaceuticals
38. Key Differences between LAF and Biological Safety Cabinet
39. Key Differences between LAF and Biological Safety Cabinet
40. Top 10 Tips for Microbial Limit Test
41. Environmental Risk from Microbial Waste
42. Computer System Validation in Pharmaceuticals
43. Ghost Peaks in Chromatography: What They Are, Why You Should Be Aware of Them
44. Best Weighing Practices in Pharmaceuticals
45. Requirement of Alarm System in Critical Equipments
46. Lux and Light Intensity for Pharmaceutical Areas
47. Different Types of HPLC Columns Used in Analysis
48. RODAC Plates and Their use in Pharmaceuticals
49. Why do We Expose Media Plates for 4 Hours in Cleanroom Areas?
50. Differences between HPLC and UPLC
51. Difference between GMP and GLP
52. Different Types of Dissolution Apparatus
53. Analyst Qualification for Quality Control Laboratory
54. Functions of Quality Control
55. Importance of Negative and Positive Controls in Microbial Analysis
56. Principle of Bacterial Endotoxin Test (BET)
57. Determination of Shelf Life of Solutions in Laboratory
58. Why Petri dishes Inverted During Incubation?
59. Principle of UV Spectrophotometer
60. Handle Microbial Cultures in Separate Room
61. Calculation for Weighing Range of Balances
62. Optical Activity in Pharmaceutical Analysis
63. Tablet Dissolution Test in Different Stages (S1, S2 and S3) Sampling Plan SQRT n+1 (√h+1) for
64. Pharmaceuticals
65. Good Laboratory Practices (GLP) Part-1
66. Good Laboratory Practices (GLP) Part-2
67. Good Laboratory Practices (GLP) Part-3
68. SOP for Out of Trend (OOT)
69. Requirements of Schedule L1 (Indian GLP) Good Laboratory Practice in Pharmaceutical
70. Good Laboratories Practice (GLP) in Pharmaceuticals
71. Update on Schedule L1
72. SOP for Good Chromatography Practices