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.

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  1. Environmental Monitoring in Pharmaceutical Cleanrooms
  2. HPLC System Suitability | Parameters & Troubleshooting
  3. How a Rotary Tablet Press Works | Complete Process
  4. HPLC Ghost Peaks | Causes & How to Fix Them
  5. Tablet Lamination | Causes, Mechanism & Remedies
  6. HPLC Carryover | Causes, Investigation & Solutions | Carry Over in HPLC
  7. Wet Granulation | Process, Stages & Critical Parameters
  8. HPLC Peak Fronting | Causes & Troubleshooting
  9. HPLC Column Selection | How to Choose the Right Column
  10. Cleanroom Classification | ISO 14644 & GMP Grades Explained
  11. HPLC Baseline Noise | Causes & Solutions
  12. Tablet Capping | Causes, Mechanism & Remedies
  13. Media Fill Failure | Investigation & CAPA Explained
  14. HPLC Peak Tailing | 10 Causes & Troubleshooting
  15. How a Fluid Bed Dryer Works | Complete Process
  16. How Tablet Coating Works | Complete Process
  17. Basics of HPLC Chromatography | HPLC Explained
  18. Types of Chromatography Explained | HPLC, GC & More
  19. Tablet Picking & Sticking: Causes and Solutions
  20. HPLC High Pressure | 7 Causes & How to Fix It
  21. How a Rapid Mixer Granulator Works | RMG Working
  22. Smoke Study in Pharma Cleanrooms: Complete Guide
  23. Change Control in Pharmaceuticals
  24. Validation of Water for Injection Loop System
  25. Tips for FDA Inspection
  26. Understanding the US FDA Drug Approval Process
  27. FDA Warning Letter - Critical cGMP Failures at Granules India Ltd
  28. ICH Guidelines Explained
  29. Understanding 21 CFR in Pharmaceuticals
  30. How to Manage Unannounced FDA Inspections
  31. 8 Common Regulatory Compliance Mistakes in Pharmaceuticals
  32. Usages of Artificial Intelligence (AI) in Pharmaceutical Industry
  33. 10 Step Guide to cGMP Certification in Pharmaceuticals
  34. Understanding Extraneous Peaks in Chromatography
  35. QC Tips for Fresh Graduates Searching for Job
  36. QC Interview Questions & Answers for Pharmaceuticals Part 2
  37. QC Interview Questions & Answers for Pharmaceuticals Part 1
  38. Working Principle of FTIR
  39. Working Principle of GC
  40. Working Principle of UV Spectrophotometer
  41. Working Principle of HPLC
  42. QA Interview Questions & Answers for Pharmaceuticals Part 2
  43. QA Interview Questions & Answers for Pharmaceuticals Part 1
  44. Equipment Failure in Pharmaceutical Manufacturing
  45. Troubleshooting Contamination Issues in Pharmaceuticals
  46. EU GMP vs FDA cGMP Key Differences
  47. FDA's Latest Guidelines for Pharma Manufacturing
  48. Regulatory Compliance:Meeting FDA Standards in Drug Manufacturing
  49. Purified Water System Validation
  50. Three Consecutive Batches for Validation
  51. Hold Time Validation Study
  52. Transport Validation
  53. How to Write a Validation Protocol
  54. Validation of Cleanroom Pass Boxes
  55. How to Reduce Validation Costs
  56. Revalidation of Purified Water System
  57. Difference between Process Validation and Product Validation
  58. How to Write a Validation Master Plan
  59. Development of Cleaning Procedure
  60. Disinfectant Validation
  61. Why is Analytical Method Validation Required
  62. Basic Requirements for Process Validation
  63. How to Effectively Execute a Validation Protocol
  64. Importance of Validation in Pharmaceuticals
  65. HPLC Method Validation
  66. Procedure for Sampling in Process Validation
  67. Stratified Sampling in Process Validation
  68. Effective Swabbing Technique for Cleaning Validation
  69. NOEL and MACO Calculations
  70. Recovery Factor of Swab
  71. Criteria to Choose the Correct Swab
  72. Regulatory Expectations for Cleaning Validation
  73. Sampling in Cleaning Validation
  74. Worst Case Selection in Cleaning Validation
  75. Cleaning Validation in 10 Steps
  76. Difference between Generic and Branded Medicines
  77. Components of GMP
  78. Fault Tree Analysis
  79. Pareto Chart for Root Cause Analysis
  80. Fishbone Diagram for Root Cause Analysis
  81. 5 Why Tool for Root Cause Analysis
  82. Top 5 Root Cause Analysis Tools
  83. Top 10 Indian Pharmaceutical Companies
  84. CAPA and Its Implementation
  85. Investigation of OOS Results
  86. Disinfectants Vs Antiseptics
  87. ALCO & ALCOA+
  88. Aseptic Vs Sterile
  89. 10 Ways to Avoid GMP Errors
  90. Difference Between Qualification and Validation
  91. Process Validation
  92. Performance Qualification
  93. Operational Qualification
  94. Installation Qualification
  95. Design Qualification
  96. Working Principle of pH Meter
  97. 6 Ways to Reduce Human Errors
  98. Different Stages of Tablet Manufacturing Process
  99. Maintenance of Aseptic Conditions in Sterile Area
  100. Air Handling Unit and Its Working
  101. GMP Violations in Indian Pharmaceutical Facilities
  102. GMP Requirements in Pharmaceuticals
  103. How to write effective SOPs
  104. How to Respond to FDA 483 Observations
  105. FDA Inspection and Compliance
  106. Self Inspection and Quality Audits
  107. Oral Liquid Dosage Forms
  108. Good Laboratory Practices (GLP)
  109. High Performance Liquid Chromatography (HPLC)
  110. Prevention of Cross-contamination in Pharmaceuticals
  111. Top 10 Tips for Microbial Limit Test
  112. Basics of HVAC Systems
  113. Steps to Minimize the Data Integrity Risk
  114. Validation Master Plan (VMP)
  115. Purpose of Process Validation
  116. Analytical Method Validation
  117. Site Acceptance Test (SAT)
  118. Top 5 Tips for Interview
  119. Tips for Telephonic Interview 
  120. Favorable Conditions for Microbial Growth in Cleanroom Area
  121. Waster Water Treatment - ETP Working
  122. Drug Master File - DMF in Pharmaceuticals
  123. Sterile Area Maintenance in Pharmaceuticals
  124. Difference between HPLC and GC │HPLC Vs GC
  125. GxP in Pharmaceuticals
  126. Validation Program in Pharmaceuticals
  127. Forced Degradation Study in Pharmaceuticals
  128. FDA Training Requirements
  129. Tips to Reduce FDA 483 Observations
  130. Top 6 Ways to Reduce Human Errors
  131. 5 Why Tool for Root Cause Investigation
  132. Fishbone Diagram Tool of Investigation
  133. Root Cause Analysis with Examples
  134. Basics of Cleaning Validation
  135. ALCOA in Pharmaceuticals
  136. Principle and Working of Autoclave
  137. Data Integrity in Pharmaceuticals
  138. Interview Questions and Answers for Jobs
  139. Good Laboratory Practices in Microbiology
  140. Quality Assurance vs Quality Control / QA vs QC
  141. Disinfectant vs Antiseptic
  142. Process Validation in Pharmaceutical Manufacturing
  143. Why do HEPA filters have 0.3 micron pore size?
  144. Good Manufacturing Practices - GMP in Pharmaceuticals
  145. Corrective and Preventive Action - CAPA
  146. Good Documentation Practices - GDP
  147. Tips to Write a Powerful CV
  148. Clean Room Design in Pharmaceuticals
  149. Air Handling Unit - AHU in Pharmaceuticals

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