Sources and Control of Contamination (single user digital version)
- Published
- Sep 2014
- Pages
- 250
- PDA Item Number
- 17970
- Format
- PDF Single user
- Member Price
- $200.00
- Nonmember Price
- $250.00
- Government Price
- $150.00
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Written by subject matter experts, these chapters are organized by topic and excerpted from volumes in the Contamination Control in Healthcare Manufacturing series
- Facility Design and Control: Personnel by Anne Marie Dixon. Chapter excerpted from Volume 1, Chapter 5 published May 2013.
- Fungal and Bacterial Spores: Contamination and Disinfection by Jim Polarine, Carol Bartnett and Dan Klein. Chapter excerpted from Volume 1, Chapter 11 published May 2013.
- Contamination Control Risk Assessment by Tim Sandle. Chapter excerpted from Volume 1, Chapter 18 published May 2013.
- Contamination Risks and the Patient by Mark Hunter, Michelle Luebke, and Mark Pasmore. Chapter excerpted from Volume 2, Chapter 4 published March 2014.
- Contamination Control in Drug Substance Manufacture by David Fletcher. Chapter excerpted from Volume 2, Chapter 12 published March 2014.
- Implementing a Contamination Control Strategy in the Biotech Industry to Effectively Maintain Microbial Contamination Control by Jane Wyatt. Chapter excerpted from Volume 2, Chapter 7 published March 2014.
- An Audit Approach to Address Microbial Contamination in Process Equipment by Paul Lopolito and Elizabeth Rivera. Chapter excerpted from Volume 1, Chapter 15 published May 2013.
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Format: PDF (1 file 1.78 MB)
About the Authors
About the Editors
Jeanne Moldenhauer, Excellent Pharma Consulting, has nearly 30 years of experience in the pharmaceutical industry. She chairs the PDA Environmental Monitoring/Microbiology Interest Group, serves on the PDA Scientific Advisory Board, founded the Rapid Microbiology User`s Group TM, and is a member of ASQ and RAPS. She is the author of Recent Warning Letters Review for Preparation of a Non-Sterile Processing Inspection, Volume 2; Recent Warning Letters Review for Preparation of an Aseptic Processing Inspection and the Editor of Environmental Monitoring: A Comprehensive Handbook Series; Steam Sterilization: A Practitioner`s Guide; Laboratory Validation: A Practitioner`s Guide; Systems Based Inspections for Pharmaceutical Manufacturers and Thermal Validation in Moist Heat Sterilization among numerous other recent publications. She is the winner of the 2010 and 2005 PDA/DHI Distinguished Editor/Author Award.
Russell Madsen, President, The Williamsburg Group, LLC, has led the organization since its founding in 2003 and has over forty-five years of experience in the pharmaceutical industry. The Williamsburg Group provides expert pharmaceutical consulting services including CGMP compliance, quality systems, aseptic processing and sterilization, sterilizing filtration, design review, due diligence and regulatory liaison.