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Review of Standard for Evaluating the Effectiveness of Contact Lens Disinfectants
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“Visually Clean” as a Sole Acceptance Criterion for Cleaning Validation Protocols
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PCR Detection of Salmonella typhimurium in Pharmaceutical Raw Materials and Products Contaminated with a Mixed Bacterial Culture Using the BAX™ System
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PDA Journal of Pharmaceutical Science and Technology September 2001, 55 (5) 286-289;
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How to Develop and Validate a Total Organic Carbon Method for Cleaning Applications
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PDA Journal of Pharmaceutical Science and Technology September 2001, 55 (5) 290-294;
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Use of Pilot Plant Facilities to Aid Validation Programs
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Investigation of a Filter Structure by Microbial Retention Studies: A Synthesis and Elaboration of Prior Findings
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One-way Distribution System for Water for Injection: Process Management, Microbiological Quality Control, and Meeting Regulatory Requirements
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Absolute or Sterilizing Grade Filtration - What is Required?
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Validation of Critical Process Input Parameters in the Production of Protein Pharmaceutical Products: A Strategy for Validating New Processes or Revalidating Existing Processes
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Enumeration of Total Viable Microorganisms in an Antibiotic Raw Material Using ChemScan® Solid Phase Cytometer
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Parenteral Drug Association, Inc.