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