Environmental Monitoring for Cleanrooms and Other Controlled Operations

IESTThis on-line presentation will provide the tools to implement and maintain a compliant and practical environmental monitoring program for cleanrooms and other controlled environments. The presentation will cover the principles of environmental monitoring of cleanrooms and other controlled operations including monitoring for microorganisms as described in IEST-RP-CC023.2: Microorganisms in Cleanrooms, guidance on implementation and maintenance of an environmental monitoring program, real-time, and rapid testing programs, and case studies reflecting the value of a robust environmental monitoring program.

Who Should Attend:
• QA/QC personnel in contamination control industries
• Production personnel in contamination control industries
• Technical support personnel in contamination control industries
• Training personnel in contamination control industries

Learning Outcomes:
• Comprehension of the requirements to implement and maintain an environmental monitoring program for cleanroom and other controlled operations.
• Recognition of the requirement to monitor for cleanroom and other controlled operations.
• Knowledge of how to evaluate data derived from various real-time and rapid test methods versus traditional test methods.

Presenter Information:
Jan Eudy is the Corporate Quality Assurance Manager for Cintas Corporation. At Cintas, Eudy serves as the technical resource for cleanroom, food, and healthcare garments and products, directs the quality system and ISO registration at all cleanroom locations, and supports validation and sterile services. She implemented and monitors the HACCP risk managment program at Cintas. She is an IEST Fellow and President Emeritus. She is an active member of other professional organizations including the International Dairy Foods Association, American Society of Clinical Pathologists, National Registry of Microbiology, American Society for Microbiology, American Society for Quality, International Society for Pharmaceutical Engineers and Parenteral Drug Association. Eudy represents Cintas on the Advisory sub-committee to the FDA for the revision of the Food Processing cGMP’s. She graduated with a degree in Medical Technology from the University of Wisconsin with graduate studies in Medical Microbiology at Creighton University. She is a Registered Medical Technologist and Specialist in Microbiology with ASCP, Registered Microbiologist with NRM in Consumer Product Testing and Quality Assurance, ISO 9000 Provisional Auditor with RAB(QSA), and Certified Quality Auditor with ASQ.
Source: IEST


  1. i will appreciate if there is a site for the complete technical requirement of clean room for pharmaceutical ang food industry

  2. lisa caldwell

    I am looking for sources for ISO14644 and ISO14698 class 7 and class 8 clean rooms, for testing and qualifying and certifying. Any workshop or conference or seminar would be greatly appreciated, in the USA around the VA, NC and DC area. Thanks

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