Environmental Monitoring - Knowing your Cleanroom


Carl Patterson, M.S. is Keynote Speaker at ComplianceKey. He has completed twelve (12) 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 has helped to insure the expectations, relate........

Overview

This webinar will provide the proper methods and techniques required to maintain a clean room per FDA and ISO regulations. By the use of viable and non-viable testing, a cleanroom can be maintained. The results collected can determine the state of control the cleanroom operates on a continuous basis. In order to maintain a cleanroom, a proper cleaning agent rotation needs to be implemented. The webinar will provide a discussion of the most appropriate cleaning agents and possible schedules for use of the cleaning agents. Trending methods in order to ensure the cleanroom is maintaining a state of control. With the use of this continuous monitoring and an adequate room cleaning program a cleanroom can be maintained to perform in accordance with ISO and FDA regulations.

Why should you attend this webinar?

This webinar will provide the proper methods and techniques required to maintain a clean room per FDA and ISO regulations. By the use of viable and non-viable testing, a cleanroom can be maintained. The results collected can determine the state of control the cleanroom operates on a continuous basis. In order to maintain a cleanroom, a proper cleaning agent rotation needs to be implemented. The webinar will provide a discussion of the most appropriate cleaning agents and possible schedules for use of the cleaning agents. Trending methods in order to ensure the cleanroom is maintaining a state of control. With the use of this continuous monitoring and an adequate room cleaning program a cleanroom can be maintained to perform in accordance with ISO and FDA regulations. 

Areas Covered in the Session:

Environmental monitoring is the process of testing cleanrooms to ensure these rooms maintain a state of control. Non-viable testing is testing done to monitor the amount of total particulates within a cleanroom. Viable testing is categorized into air and surface monitoring. The viable air monitoring can be further divided into passive monitoring and active monitoring. Cleaning agents are used to lower the amount of viables within a room and increased usage can be done during contamination events.

Who can Benefit:



Webinar Id: LSHCCPA001

Training Options:

Duration: 60 mins

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 Recorded: [Six month unlimited access]

 $167 (Single Attendee)  $599 (Unlimited Attendee)

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