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

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