GOOD VALIDATION PRACTICE (cGVP)
About the CLEANING VALIDATION category
The Main Risks of Glove Damage Inside an Isolator
Top 5 Factors to Consider When Designing a Cleaning Process
It is Possible to Validate Cleaning of Cosmetic Products by Liquid Form and Vice Versa?
How Do I Set Up a Validation for a Clean/Dirty Hold Time?
Hold time studies in cleaning validation
Same equipment for manufacturing Liquid and semi solid product
Alert / Action Limit in Cleaning Validation
Approach: evaluation of Detergent, carry over calculation
Clean,Dirty Equipment Hold time study
Is CSV Required for Autoclave, Labeling Machine?
Stainless Steel Plate for Swab Recovery
What Percentage of Isopropyl Alcohol Can Be Used?
Degradation Study Large Biomolecule
CV implementation in Non Sterile API mfg facility
Dissolution Test Acceptance Criteria
Matrixing Criteria for 24 APIs
Swab alert limits and mean contaminationrecovery rates
MACO calculation - new approach
Moist heat sterilization
Treatment of Vial with HCl
Cleaning of Filling Needles Only
Is the riboflavin a good method for cleaning validation?
SOP of cleaning for Saccharomyces boulardii
Same cleaning procedure
Citric Acid as cleaning agent "in house made"
Cleaning Validation query
Validation desinfection cleanroom
next page →