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About the PROCESS VALIDATION category
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|
0
|
1375
|
February 8, 2016
|
|
Requalification Clean Compressed Air
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|
0
|
1022
|
September 9, 2019
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Minimizing the Risk of Cross Contamination in a Pharmaceutical Central Chemicals Dispensing Room
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13
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6459
|
July 17, 2018
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|
Process Validation Protocol for Soft Gelatin Capsule
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3
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3931
|
July 17, 2018
|
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Process Validation of Oral Liquid
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22
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7618
|
July 5, 2018
|
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Continued Process Verification
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23
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3984
|
June 18, 2018
|
|
Validation of Depyrogenation Cycle
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|
4
|
2182
|
June 18, 2018
|
|
Blending Validation
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|
5
|
9574
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June 1, 2018
|
|
Why Process Validation is Reliant on a Detailed Design Review of the Product [Video]
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0
|
1058
|
April 30, 2018
|
|
Comparison Report for API
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2
|
1761
|
March 7, 2018
|
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The 3 Phases of Process Validation to Ensure Quality, Safety & Efficacy [Video]
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0
|
1177
|
February 1, 2018
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|
Particulate expectations for SUTs
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|
0
|
1109
|
December 20, 2017
|
|
Process validation (brackiting)
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|
4
|
2389
|
June 19, 2017
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Validation of Packaging
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|
11
|
4298
|
June 19, 2017
|
|
Qualification and Calibration Status in Process Validation Protocol
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|
9
|
2744
|
June 3, 2017
|
|
Process Simulation - API (Mediafill)
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|
5
|
2535
|
June 1, 2017
|
|
Are Three Successful Runs for Process Validation Allowed?
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|
4
|
2910
|
June 1, 2017
|
|
Compression Air Qualification
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|
7
|
4105
|
November 17, 2016
|
|
Do you repeat process validation after change of API manufacturer?
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|
6
|
6880
|
September 13, 2016
|
|
Process optimization study
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|
7
|
3216
|
September 6, 2016
|
|
QbD
|
|
1
|
1634
|
September 2, 2016
|
|
Leak Test for Capped Bottles/Vials
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|
21
|
11385
|
June 20, 2016
|
|
Justification for Hardness OOS
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|
7
|
3881
|
May 18, 2016
|
|
Granulation End Point
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|
4
|
4190
|
May 12, 2016
|
|
Life Cycle Approach - Process Validation
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|
1
|
1786
|
May 4, 2016
|
|
Prospective validation of FDF (ointment) production
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|
9
|
2764
|
April 7, 2016
|
|
Checking volume of prepared tablet coating solution before its application
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|
9
|
3012
|
March 15, 2016
|
|
Why should we use 46.4 as z value in dry sterilzation as recommended z value of dry amps r 29?give me xvt rationale for this?
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2
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2631
|
February 19, 2016
|
|
Process validation of a tablet product
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|
3
|
2077
|
December 2, 2015
|
|
Validation Master Plan
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|
1
|
1786
|
August 7, 2015
|