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|Articles|November 1, 1999

LCGC North America

  • November 1999
  • Volume 17
  • Issue 11
  • Pages: 1016–1019

Cleaning Validation

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

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

almost 27 years ago

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

almost 27 years ago

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

almost 27 years ago

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

almost 27 years ago

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

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