|
About the PROCESS VALIDATION category
|
|
0
|
1279
|
February 8, 2016
|
|
Requalification Clean Compressed Air
|
|
0
|
888
|
September 9, 2019
|
|
Process Validation Protocol for Soft Gelatin Capsule
|
|
3
|
3543
|
July 17, 2018
|
|
Minimizing the Risk of Cross Contamination in a Pharmaceutical Central Chemicals Dispensing Room
|
|
13
|
6196
|
July 17, 2018
|
|
Process Validation of Oral Liquid
|
|
22
|
6925
|
July 5, 2018
|
|
Validation of Depyrogenation Cycle
|
|
4
|
2059
|
June 18, 2018
|
|
Continued Process Verification
|
|
23
|
3755
|
June 18, 2018
|
|
Blending Validation
|
|
5
|
9303
|
June 1, 2018
|
|
Why Process Validation is Reliant on a Detailed Design Review of the Product [Video]
|
|
0
|
964
|
April 30, 2018
|
|
Comparison Report for API
|
|
2
|
1646
|
March 7, 2018
|
|
The 3 Phases of Process Validation to Ensure Quality, Safety & Efficacy [Video]
|
|
0
|
1066
|
February 1, 2018
|
|
Particulate expectations for SUTs
|
|
0
|
975
|
December 20, 2017
|
|
Process validation (brackiting)
|
|
4
|
2248
|
June 19, 2017
|
|
Validation of Packaging
|
|
11
|
4071
|
June 19, 2017
|
|
Qualification and Calibration Status in Process Validation Protocol
|
|
9
|
2620
|
June 3, 2017
|
|
Process Simulation - API (Mediafill)
|
|
5
|
2411
|
June 1, 2017
|
|
Are Three Successful Runs for Process Validation Allowed?
|
|
4
|
2760
|
June 1, 2017
|
|
Compression Air Qualification
|
|
7
|
3977
|
November 17, 2016
|
|
Do you repeat process validation after change of API manufacturer?
|
|
6
|
6720
|
September 13, 2016
|
|
Process optimization study
|
|
7
|
3108
|
September 6, 2016
|
|
QbD
|
|
1
|
1508
|
September 2, 2016
|
|
Leak Test for Capped Bottles/Vials
|
|
21
|
11006
|
June 20, 2016
|
|
Justification for Hardness OOS
|
|
7
|
3732
|
May 18, 2016
|
|
Granulation End Point
|
|
4
|
4041
|
May 12, 2016
|
|
Life Cycle Approach - Process Validation
|
|
1
|
1681
|
May 4, 2016
|
|
Prospective validation of FDF (ointment) production
|
|
9
|
2632
|
April 7, 2016
|
|
Checking volume of prepared tablet coating solution before its application
|
|
9
|
2891
|
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?
|
|
2
|
2418
|
February 19, 2016
|
|
Process validation of a tablet product
|
|
3
|
1950
|
December 2, 2015
|
|
Validation Master Plan
|
|
1
|
1665
|
August 7, 2015
|