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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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