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About the CLEANING VALIDATION category
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1
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1369
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February 8, 2016
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OQ & PQ of Vial washing Machine
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6
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979
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August 26, 2020
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Die to Die should be used to validate the CIP process
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5
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989
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May 22, 2020
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Maximum daily dose for topical products
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3
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624
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October 14, 2019
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Cleaning's Validation for alcohol based product
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5
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769
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August 20, 2019
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Safe for use or no
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2
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762
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May 20, 2019
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Defining MACO parameters
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2
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836
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May 16, 2019
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PQ/Cleaning validation vial washer
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5
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1348
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April 5, 2019
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How Do I Set Up a Validation for a Clean/Dirty Hold Time?
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24
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11250
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March 31, 2019
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Prerequisites for visual inspector
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2
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808
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March 14, 2019
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Total Organic Carbon
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3
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919
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March 13, 2019
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Lab ware cleaning validation
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13
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2869
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February 6, 2019
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Stainless Steel Plate for Swab Recovery
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7
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3939
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December 26, 2018
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The Main Risks of Glove Damage Inside an Isolator
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1
|
883
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August 22, 2018
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Top 5 Factors to Consider When Designing a Cleaning Process
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1
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854
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August 20, 2018
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It is Possible to Validate Cleaning of Cosmetic Products by Liquid Form and Vice Versa?
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13
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2897
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July 19, 2018
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Same equipment for manufacturing Liquid and semi solid product
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15
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2236
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June 11, 2018
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Hold time studies in cleaning validation
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2
|
1304
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June 10, 2018
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Alert / Action Limit in Cleaning Validation
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|
5
|
1608
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May 26, 2018
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Approach: evaluation of Detergent, carry over calculation
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1
|
968
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April 12, 2018
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Clean,Dirty Equipment Hold time study
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16
|
9995
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March 27, 2018
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Is CSV Required for Autoclave, Labeling Machine?
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1
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916
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February 28, 2018
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What Percentage of Isopropyl Alcohol Can Be Used?
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10
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2496
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February 8, 2018
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Degradation Study Large Biomolecule
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5
|
1172
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February 6, 2018
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CV implementation in Non Sterile API mfg facility
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5
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1964
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January 26, 2018
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Dissolution Test Acceptance Criteria
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3
|
1541
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January 16, 2018
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Matrixing Criteria for 24 APIs
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11
|
2398
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January 4, 2018
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Swab alert limits and mean contaminationrecovery rates
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3
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1002
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December 21, 2017
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MACO calculation - new approach
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16
|
3104
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December 16, 2017
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Moist heat sterilization
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4
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1252
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November 1, 2017
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