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Validation

  1. Difference Between Concurrent, Prospective, and Retrospective Validation
  2. Concurrent Validation in Pharmaceutical Manufacturing: A Comprehensive Overview
  3. Retrospective Validation for Pharmaceutical Manufacturing: An Overview
  4. Prospective Validation in Pharmaceutical Manufacturing: An In-Depth Guide
  5. Procedures (SOP) for Bubble Point Test for Filters: A Comprehensive Guide
  6. Procedures (SOP) for Forward Flow Test (Diffusion Test) for Filters: A Comprehensive Guide
  7. Procedures (SOP) for Pressure Hold Test for Filters: A Comprehensive Guide
  8. Procedures (SOP) for Water Intrusion Test for Filters: A Comprehensive Guide
  9. Procedures (SOP) for Filters Integrity Test Using Aerosols: A Comprehensive Guide
  10. Standard Operating Procedure (SOP) for In-House Trial Procedure in a Pharmaceutical Analytical Laboratory
  11. Standard Operating Procedure (SOP) for Validation of Deviation Management in Analytical Laboratory
  12. Standard Operating Procedure (SOP) for Cleaning, Derouging, and Passivation of Stainless Steel Parts of a Purified Water System
  13. Standard Operating Procedure (SOP) for In-House Trial Procedure in a Pharmaceutical Manufacturing Firm
  14. Standard Operating Procedure (SOP) for Calibration Procedure (Ice Point) for Thermometers and Thermocouples
  15. Installation Qualification: A Cornerstone of Quality in Regulated Industries
  16. How to Complete Installation Qualification: A Step-by-Step Guide
  17. Drafting a Robust Installation Qualification Protocol
  18. Operational Qualification (OQ) vs. Performance Qualification (PQ) in Validation
  19. Performing Operational Qualification: A Step-by-Step Guide
  20. Operational Qualification of Utilities in Pharmaceuticals
  21. Operational Qualification of an Autoclave
  22. Operational Qualification of a Tablet Compression Machine
  23. Operational Qualification of a Purified Water System
  24. Operational Qualification of an HPLC Instrument
  25. Operational Qualification of an HVAC System
  26. Operational Qualification of Software
  27. Operational Qualification of Pipework Systems in Pharmaceuticals
  28. Analytical Method Validation: An Overview
  29. Performance Parameters Required for Assay Validation
  30. Standard Operating Procedure (SOP) – Validation: Concept and Procedure
  31. Standard Operating Procedure For Revalidation Procedure
  32. Equipment Specification and Qualification in Pharmaceutical Firms
  33. Validation of Laboratory Instruments
  34. Validation of Compressed Air
  35. Validation of the Effectiveness of UV Light in Water Systems in the Pharmaceutical Industry
  36. Mastering Cleaning Validation for Laboratory Glassware: A Step-by-Step Protocol for Analytical Labs
  37. Validation Master Plan (VMP) for Pharmaceutical Industry Warehouse
  38. Three Consecutive Batches for Validation in Pharmaceuticals Qualification Procedure for Vial Washing Machine
  39. HPLC System Software Validation Plan
  40. NOEL and MACO Calculations in Cleaning Validation Purpose of Process Validation in Pharmaceuticals
  41. Recovery Factor Determination in Cleaning Validation Sampling in Cleaning Validation in Pharmaceutical
  42. Industry Cleaning Validation of Clean-in-Place (CIP) Systems Importance of Validation in Pharmaceuticals
  43. Regulatory Expectations from Cleaning Validation
  44. How to Effectively Execute a Validation Protocol?
  45. How to Write a Validation Master Plan?
  46. Revalidation of Equipment and Process in Pharmaceuticals
  47. Alarm Challenge Test in Pharmaceuticals
  48. Steps for HPLC Method Validation
  49. Design Qualification (DQ) of Equipment
  50. Performance Qualification (PQ) of Pharmaceutical Equipment
  51. Operational Qualification (OQ) in Pharmaceuticals
  52. Installation Qualification (10) in Pharmaceuticals
  53. Validation of Fumigation in Cleanroom Area
  54. Revalidation of Pharmaceutical Processes
  55. Validation of the Effectiveness of UV Light in Water System
  56. Media Fill Test for Sterile API Manufacturing Process
  57. How to Write a Validation Protocol?
  58. Why is Analytical Method Validation Required?
  59. Identification of Worst Case in Cleaning Validation
  60. Purified Water System Validation
  61. Procedure for Sampling in Process Validation
  62. Validation of Clean Room Pass Boxes
  63. Validation Program in Pharmaceutical Industries
  64. Tips to Develop Equipment Cleaning Procedure
  65. Basics of Cleaning Validation
  66. Validation of Utility Systems in Pharmaceutical Facilities
  67. Low Temperature Sterilization Process (115°C) and Its Validation
  68. Basic Requirements for Process Validation Exercise
  69. Factory Acceptance Test – FAT
  70. Concept of GAMP 5 in Pharmaceuticals Media Fill Test Failure Investigation
  71. Cleaning Validation of Pharmaceutical Equipment
  72. Reduce Validation Cost in Pharmaceuticals
  73. FDA Warning Letters for Cleaning Validation Computerized System Validation Planning and Execution
  74. The Stratified Sampling Approach in Process Validation
  75. Regulatory Requirements and Guidelines for Cleaning Validation Criteria to Choose the Correct Swab for
  76. Cleaning Validation
  77. Transport Validation for Pharmaceutical Products
  78. Procedure for Process Validation in Pharmaceuticals
  79. What is Disinfectant Validation?
  80. Aseptic Filling Process (Media Fill) Validation Protocol in Sterile Pharmaceuticals
  81. Process Validation in Pharmaceutical Manufacturing
  82. Hold Time Study in Pharmaceutical Manufacturing
  83. Re-validation of Purified Water System
  84. Importance of Cleaning Validation in Pharmaceutical Manufacturing
  85. Difference between Process Validation and Product Validation
  86. Is It Possible to Switch off HVAC System in Night?
  87. Cleaning Method Validation Protocol for Pharmaceutical Equipments
  88. Cleaning Validation Sample Protocol
  89. Difference among Calibration, Validation & Qualification
  90. SOP for Personnel Gowning Qualification
  91. SOP for Validation of Clean Area and Equipment Lying in Clean Area
  92. SOP for Heating Block Validation
  93. SOP for Validation of Autoclave with Biological Indicators
  94. SOP for Validation of Microbiologist
  95. SOP for Analyst Validation/ Qualification in Quality Control
  96. SOP for Swab Sampling for Validation of Test Surface to Evaluate Cleaning Efficacy.
  97. SOP for Computer Systern Validation
  98. SOP for Validation of Autoclave with Biological Indicator for Sterilization Efficiency SOP for Validation of Autoclave
  99. Analyst Qualification for Quality Control Laboratory
  100. Qualification of Calculator
  101. Disinfectant Validation Protocol
  102. Sterile Area (Cleanroom) Qualification
  103. Sampling and Testing in Exhibit and Process Validation Batches
  104. Analytical Method Development Process for New Products
  105. Validation of Pure Steam
  106. Process Validation Sample Protocol
  107. Analytical Method Validation Protocol for Pharmaceuticals
  108. Validation Protocol for Hold Time Study of Collected Water Samples
  109. Performance Qualification Protocol for Water for Injection (WFI) System
  110. Now Verify Sterilization Process in Two Hours with New Genetically Engineered Biological Indicators
  111. Validation Protocol for Hold Time Study of Swab Test Samples
  112. Hold Time Study Protocol of Sterilized Garments for their Sterility
  113. Validation Protocol for Hold Time Study of Sterilized Glassware and Accessories
  114. Validation Protocol for Hold Time Study of Prepared Inoculum Suspension
  115. Validation Protocol for Efficacy of Chemical Disinfectants
  116. Validation Protocol to Determine the Shelf Life of Prepared Microbiological Media
  117. Cleaning Validation Protocol for Sample Container
  118. Water for Injection (WFI) System Validation Process
  119. Heating, Ventilation and Air Conditioning (HVAC) System Validation Process
  120. Autoclave (Steam Sterilizer) Validation
  121. Validation of Excel Calculation Sheets
  122. Guidelines for Preparation of VMP (Validation Master Plan)
  123. Analytical Method Validation
  124. Concept of Revalidation in Pharmaceuticals
  125. Non-sterile Process Validation in Pharmaceuticals
  126. Analytical Method Validation Definitions in Pharmaceuticals
  127. Cleaning Validation of Manufacturing Equipment
  128. Validation of Supporting Processes in Pharmaceuticals Transport Validation Sample Protocol
  129. WHO Qualification List for Pharmaceutical Equipments
  130. Qualification of Systems and Equipment in Pharmaceuticals Cleaning Validation Protocol for Pharmaceuticals
  131. Prospective Validation
  132. Validation of Shelf Life for 70% v/v Isopropyl Alcohol (IPA)
  133. Performance Qualification of High Pressure High Vaccum (HPHV) Steam Sterilizer in Pharmaceuticals
  134. Performance Qualification of Autoclave cum Bung Processor
  135. Hold Time Study of Cleaned Equipments
  136. Performance Evaluation of Biological Indicators
  137. Facility Qualification in Pharmaceuticals
  138. Procedure for Qualification of Vendors for Raw Material and Packaging Materials
  139. Facility Qualification in Pharmaceuticals
  140. Procedure for Qualification of Vendors for Raw Material and Packaging Materials Sterility Validation
  141. (Membrane Filtration Method) in Pharmaceuticals
  142. Media Fill Validation -SVP
  143. Bacterial Endotoxin Test (BET or LAL Test) Method Validation
  144. FDA’s New Process Validation Guidance
  145. MLT (Microbial Limit Test) Validation
  146. Validation of Dry Heat Sterilizer (DHS)
  147. Media Fill Validation Test in Sterile Pharmaceutical
  148. Protocol for Hold Time Study of Prepared Control Standard Endotoxin (CSE)