About the GOOD DOCUMENTATION PRACTICE (GDocP) category
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0
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1340
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February 8, 2016
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Fixed parameter or not?
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6
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390
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September 13, 2021
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autoclave
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6
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3616
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April 2, 2021
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Steam Sterilization Lethality (Fo) Calculation
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5
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12298
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February 26, 2021
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IQ Execution Ownership for SAP system
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4
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1022
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March 22, 2019
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PQ of pure steam
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8
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3883
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February 28, 2019
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OQ Server
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1
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1023
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January 26, 2019
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Release Notes Assessment
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0
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731
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January 17, 2019
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Repetitive Deviation
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3
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1832
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November 10, 2018
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What do you do when a critical deviation is performed?
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1
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879
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November 9, 2018
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Difference between SAT and IQ/OQ
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9
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8427
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August 28, 2018
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DIP - Deviation investigation protocol: responsibilities
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17
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2655
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August 28, 2018
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Dynamic pass box- Functional Requirement
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9
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9417
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August 28, 2018
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At What Stage Should We Write our VMP?
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7
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2765
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July 19, 2018
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What is an RTM?
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5
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3893
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June 25, 2018
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Element of handwritten signature
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0
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1245
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June 18, 2018
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OQ Protocol for Blister Sealing Machine
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8
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3205
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June 11, 2018
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10 Best Practices for Creating Solid User Requirements [Video]
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0
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874
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April 17, 2018
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10 Things You Need to Know About Creating User Requirements
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0
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891
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March 27, 2018
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The Main Deliverables of a Validation Master Plan (VMP) [Video]
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0
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810
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March 27, 2018
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Please share your words on FAT/SAT/UAT and IQ/OQ/PQ
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3
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5468
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March 13, 2018
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Process Validation & Cleaning Validation
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4
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1902
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March 8, 2018
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Design Qualification - PLC
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5
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3735
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March 1, 2018
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FAT, SAT Application
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16
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6082
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February 21, 2018
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Assay Method validation, Recovery(Accuracy)
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1
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1310
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February 6, 2018
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Action Limits above Specifications
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7
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1726
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January 15, 2018
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Annual Product Review Report Outline
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3
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2206
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January 10, 2018
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Type I Lab Water Purification System Specs
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8
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1836
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October 25, 2017
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URS Examples for Cold Room and Warehouse Air Conditioning System
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1
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1954
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September 22, 2017
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Performance Qualification of Fluid Bed Dryer
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3
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3264
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September 8, 2017
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