|
About the CLEANING VALIDATION category
|
|
0
|
1461
|
February 8, 2016
|
|
Carryover limit for filter bags?
|
|
0
|
41
|
May 22, 2021
|
|
How should I determine MACO formula for Topical Solution?
|
|
0
|
145
|
March 9, 2021
|
|
OQ & PQ of Vial washing Machine
|
|
5
|
1227
|
August 26, 2020
|
|
Die to Die should be used to validate the CIP process
|
|
4
|
1236
|
May 22, 2020
|
|
What is the maximum daily dose for topical products?
|
|
2
|
852
|
October 14, 2019
|
|
Cleaning's Validation for alcohol based product
|
|
4
|
929
|
August 20, 2019
|
|
Safe for use or no
|
|
1
|
855
|
May 20, 2019
|
|
Defining MACO parameters
|
|
1
|
964
|
May 16, 2019
|
|
PQ/Cleaning validation vial washer
|
|
4
|
1752
|
April 5, 2019
|
|
How Do I Set Up a Validation for a Clean/Dirty Hold Time?
|
|
23
|
11893
|
March 31, 2019
|
|
Prerequisites for visual inspector
|
|
1
|
910
|
March 14, 2019
|
|
Total Organic Carbon
|
|
2
|
1073
|
March 13, 2019
|
|
Lab ware cleaning validation
|
|
12
|
3082
|
February 6, 2019
|
|
Stainless Steel Plate for Swab Recovery
|
|
6
|
4271
|
December 26, 2018
|
|
The Main Risks of Glove Damage Inside an Isolator
|
|
0
|
988
|
August 22, 2018
|
|
Top 5 Factors to Consider When Designing a Cleaning Process
|
|
0
|
948
|
August 20, 2018
|
|
It is Possible to Validate Cleaning of Cosmetic Products by Liquid Form and Vice Versa?
|
|
12
|
3203
|
July 19, 2018
|
|
Same equipment for manufacturing Liquid and semi solid product
|
|
14
|
2386
|
June 11, 2018
|
|
Hold time studies in cleaning validation
|
|
1
|
1392
|
June 10, 2018
|
|
Alert / Action Limit in Cleaning Validation
|
|
4
|
1751
|
May 26, 2018
|
|
Approach: evaluation of Detergent, carry over calculation
|
|
0
|
1055
|
April 12, 2018
|
|
Clean,Dirty Equipment Hold time study
|
|
15
|
10597
|
March 27, 2018
|
|
Is CSV Required for Autoclave, Labeling Machine?
|
|
0
|
1100
|
February 28, 2018
|
|
What Percentage of Isopropyl Alcohol Can Be Used?
|
|
9
|
2638
|
February 8, 2018
|
|
Degradation Study Large Biomolecule
|
|
4
|
1260
|
February 6, 2018
|
|
CV implementation in Non Sterile API mfg facility
|
|
4
|
2057
|
January 26, 2018
|
|
Dissolution Test Acceptance Criteria
|
|
2
|
1686
|
January 16, 2018
|
|
Matrixing Criteria for 24 APIs
|
|
10
|
2510
|
January 4, 2018
|
|
Swab alert limits and mean contaminationrecovery rates
|
|
2
|
1098
|
December 21, 2017
|
