Can Anyone told me how to write empty chamber temperature mapping for autoclave
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1
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1371
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May 27, 2013
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WFI system qualification
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1
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1796
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May 21, 2013
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Validation Deviations – An Important Part of Any Validation Project
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0
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1455
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May 20, 2013
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Product Contact Materials Requirement
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7
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2837
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May 3, 2013
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Product, Material, Personnel, Waste Flow Diagram
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2
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1819
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April 29, 2013
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Inprocess/validation measurement systems
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0
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1047
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February 26, 2013
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Facility Qualification
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3
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1473
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February 20, 2013
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Showing Insufficient Deviations to Support Comprehensive Testing
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0
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1229
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February 5, 2013
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HPLC Performance Qualification
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9
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6187
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January 31, 2013
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Training Checklist
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4
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2681
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January 24, 2013
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Drawing Schedule Template
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0
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1083
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January 11, 2013
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Validation Activity Plan
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0
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1243
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January 11, 2013
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cGMP Impact Assessment
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0
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1172
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January 11, 2013
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Validation procedure for HPLC Waters 2695
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0
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1407
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December 19, 2012
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Technology Transfer
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3
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1110
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December 18, 2012
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Pq of stainless steel reactor
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0
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1757
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December 15, 2012
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Biofermentor Validation
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0
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1087
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December 13, 2012
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Validation Policy
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1
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1379
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December 10, 2012
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Validation approach
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4
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1542
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December 5, 2012
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Toc samples
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1
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1305
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December 5, 2012
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Validation Summary Report Outline based on PIC/S
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0
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1265
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November 24, 2012
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DQ Outline Protocol based on PIC/S
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0
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1092
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November 24, 2012
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PQ Protocol Outline based on PIC/S
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0
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1118
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November 24, 2012
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OQ Protocol Outline based on PIC/S
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0
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1330
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November 24, 2012
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IQ Protocol based on PIC/S Guidelines
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0
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1171
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November 24, 2012
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Qualification vs Validation
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3
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1259
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November 20, 2012
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PQ of pure steam
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6
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2048
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November 17, 2012
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Document revision status
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4
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1265
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November 7, 2012
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Isolater validaton
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6
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2442
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October 29, 2012
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Managing Requirements Throughout Multiple Life Cycle Stages
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0
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1279
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October 23, 2012
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