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Attendees will get an overview of environmental monitoring investigations and tools to complete an investigation. Environmental monitoring is the method by which clean rooms are known to maintain a certain level of cleanliness. The methods by which clean rooms are monitored are through viable and non-viable testing. Through this testing, a room may demonstrate that it is out of control. This seminar will provide aspects to investigate in order to determine a root cause and appropriate actions to complete the report.

Why Should You Attend:

Regulatory agencies review environmental monitoring programs to determine how well a facility is in a state of control. Excursions related to environmental monitoring are crucial in demonstrating this to an auditor. Investigations as results of environmental monitoring must be thorough and have the proper corrective actions put into place. The purpose of this webinar is to demonstrate how to conduct a thorough investigation and determine the proper actions to take as a result of the investigation.

Areas Covered in this Webinar:

Topics covered include:

International regulations (ISO)
Federal regulation (FDA, USP)
Non-viable testing
Viable testing
Identification of microorganisms
Possible sources
Determination of a root cause
Corrective and Preventative actions to put into place

Learning Objectives:

Environmental monitoring of clean rooms is a key component in demonstrating a pharmaceutical manufacturing facility is in a state of control. However, when environmental monitoring excursions occur, it can prove something within the system is amiss. By having a through environmental monitoring investigation, root causes and corrective actions can be put into place to demonstrate the facility is under control. This webinar will give an understanding of environmental monitoring, approaches to resolving excursions, and putting the proper corrective and preventative actions into place to reduce future excursions.

Who Will Benefit:

All personnel who work for pharmaceutical manufacturing and contract manufacturing organizations where environmental monitoring is done.

Speaker Profile:

Carl Patterson, M.S. has completed twelve (13) plus years in the biotechnology, pharmaceutical manufacturing, and quality fields. He completed his Bachelor’s of Science in Microbiology from the University of Texas.

Also, has completed specialized certificates in biotechnology manufacturing, quality control, and quality assurance from UCSD, and has completed his Master’s of Science in Biomedical Quality Systems from SDSU. Through the years, has worked with several companies in regards to aseptic processing and environmental monitoring. He has helped to insure the expectations, related to aseptic processing and environmental monitoring, have been met.

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