Pharmaceutical Videos

Any topic can be understood better with the videos, so we are working hard to create videos of important topics to help the students and professionals. Here is the list of videos created by Pharmaguideline.

We update this list regularly.

1. Working Principle of GC
2. Working Principle of UV Spectrophotometer
3. Working Principle of HPLC
4. QA Interview Questions & Answers for Pharmaceuticals Part 2
5. QA Interview Questions & Answers for Pharmaceuticals Part 1
6. Equipment Failure in Pharmaceutical Manufacturing
7. Troubleshooting Contamination Issues in Pharmaceuticals
8. EU GMP vs FDA cGMP Key Differences
9. FDA's Latest Guidelines for Pharma Manufacturing
10. Regulatory Compliance:Meeting FDA Standards in Drug Manufacturing
11. Purified Water System Validation
12. Three Consecutive Batches for Validation
13. Hold Time Validation Study
14. Transport Validation
15. How to Write a Validation Protocol
16. Validation of Cleanroom Pass Boxes
17. How to Reduce Validation Costs
18. Revalidation of Purified Water System
19. Difference between Process Validation and Product Validation
20. How to Write a Validation Master Plan
21. Development of Cleaning Procedure
22. Disinfectant Validation
23. Why is Analytical Method Validation Required
24. Basic Requirements for Process Validation
25. How to Effectively Execute a Validation Protocol
26. Importance of Validation in Pharmaceuticals
27. HPLC Method Validation
28. Procedure for Sampling in Process Validation
29. Stratified Sampling in Process Validation
30. Effective Swabbing Technique for Cleaning Validation
31. NOEL and MACO Calculations
32. Recovery Factor of Swab
33. Criteria to Choose the Correct Swab
34. Regulatory Expectations for Cleaning Validation
35. Sampling in Cleaning Validation
36. Worst Case Selection in Cleaning Validation
37. Cleaning Validation in 10 Steps
38. Difference between Generic and Branded Medicines
39. Components of GMP
40. Fault Tree Analysis
41. Pareto Chart for Root Cause Analysis
42. Fishbone Diagram for Root Cause Analysis
43. 5 Why Tool for Root Cause Analysis
44. Top 5 Root Cause Analysis Tools
45. Top 10 Indian Pharmaceutical Companies
46. CAPA and Its Implementation
47. Investigation of OOS Results
48. Disinfectants Vs Antiseptics
49. ALCO & ALCOA+
50. Aseptic Vs Sterile
51. 10 Ways to Avoid GMP Errors
52. Difference Between Qualification and Validation
53. Process Validation
54. Performance Qualification
55. Operational Qualification
56. Installation Qualification
57. Design Qualification
58. Working Principle of pH Meter
59. 6 Ways to Reduce Human Errors
60. Different Stages of Tablet Manufacturing Process
61. Maintenance of Aseptic Conditions in Sterile Area
62. Air Handling Unit and Its Working
63. GMP Violations in Indian Pharmaceutical Facilities
64. GMP Requirements in Pharmaceuticals
65. How to write effective SOPs
66. How to Respond to FDA 483 Observations
67. FDA Inspection and Compliance
68. Self Inspection and Quality Audits
69. Oral Liquid Dosage Forms
70. Good Laboratory Practices (GLP)
71. High Performance Liquid Chromatography (HPLC)
72. Prevention of Cross-contamination in Pharmaceuticals
73. Top 10 Tips for Microbial Limit Test
74. Basics of HVAC Systems
75. Steps to Minimize the Data Integrity Risk
76. Validation Master Plan (VMP)
77. Purpose of Process Validation
78. Analytical Method Validation
79. Site Acceptance Test (SAT)
80. Top 5 Tips for Interview
81. Tips for Telephonic Interview 
82. Favorable Conditions for Microbial Growth in Cleanroom Area
83. Waster Water Treatment - ETP Working
84. Drug Master File - DMF in Pharmaceuticals
85. Sterile Area Maintenance in Pharmaceuticals
86. Difference between HPLC and GC │HPLC Vs GC
87. GxP in Pharmaceuticals
88. Validation Program in Pharmaceuticals
89. Forced Degradation Study in Pharmaceuticals
90. FDA Training Requirements
91. Tips to Reduce FDA 483 Observations
92. Top 6 Ways to Reduce Human Errors
93. 5 Why Tool for Root Cause Investigation
94. Fishbone Diagram Tool of Investigation
95. Root Cause Analysis with Examples
96. Basics of Cleaning Validation
97. ALCOA in Pharmaceuticals
98. Principle and Working of Autoclave
99. Data Integrity in Pharmaceuticals
100. Interview Questions and Answers for Jobs
101. Good Laboratory Practices in Microbiology
102. Quality Assurance vs Quality Control / QA vs QC
103. Disinfectant vs Antiseptic
104. Process Validation in Pharmaceutical Manufacturing
105. Why do HEPA filters have 0.3 micron pore size?
106. Good Manufacturing Practices - GMP in Pharmaceuticals
107. Corrective and Preventive Action - CAPA
108. Good Documentation Practices - GDP
109. Tips to Write a Powerful CV
110. Clean Room Design in Pharmaceuticals
111. Air Handling Unit - AHU in Pharmaceuticals
     

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