Cleaning Validation

Author(s)Ira S. Krull, Michael E. Swartz

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

almost 27 years ago

Article

Monoliths as Stationary Phases for Separating Biopolymers – Fourth-Generation Chromatography Sorbents

almost 27 years ago

Article

Automated DNA Fragment Analysis by High Performance Ultrathin-Layer Agarose Gel Electrophoresis

almost 27 years ago

Article

A Coin-Toss Experiment, Part II – Limits of the Analogy

almost 27 years ago

Article

Ion-Exchange Displacement Chromatography: Scale-Up and Displacer Clearance for Recombinant Human Brain-Derived Neurotrophic Factor

almost 27 years ago

Article

Readers' Question – Carryover, Mobile-Phase Temperature, and Column Care

Newsletter

Join the global community of analytical scientists who trust LCGC for insights on the latest techniques, trends, and expert solutions in chromatography.