Cleaning Validation

Publication
Article
LCGC North AmericaNovember 1999
Volume 17
Issue 11
Pages: 1016–1019

Krull and Swartz examine validating cleaning methods for pharmaceutical manufacturing equipment and look at general requirements and specific cleaning procedures, sampling types, and analytical methods.

This month's column looks at validating cleaning methods for pharmaceutical manufacturing equipment. Krill and Swartz discuss general requirements and specific cleaning procedures, sampling types, and analytical methods.

LCGC 17(11), 1016–1019 (1999).
Articles in this issue
Monoliths as Stationary Phases for Separating Biopolymers – Fourth-Generation Chromatography Sorbents
Monoliths as Stationary Phases for Separating Biopolymers – Fourth-Generation Chromatography Sorbents
Automated DNA Fragment Analysis by High Performance Ultrathin-Layer Agarose Gel Electrophoresis
Automated DNA Fragment Analysis by High Performance Ultrathin-Layer Agarose Gel Electrophoresis
A Coin-Toss Experiment, Part II – Limits of the Analogy
A Coin-Toss Experiment, Part II – Limits of the Analogy
Ion-Exchange Displacement Chromatography: Scale-Up and Displacer Clearance for Recombinant Human Brain-Derived Neurotrophic Factor
Ion-Exchange Displacement Chromatography: Scale-Up and Displacer Clearance for Recombinant Human Brain-Derived Neurotrophic Factor
wrench and gear
Readers' Question – Carryover, Mobile-Phase Temperature, and Column Care
Cleaning Validation
Cleaning Validation
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