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

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