2021 - Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers

There are seven (7) key topics that will be discussed on Day 1 and Day 2 of the Seminar are as follows:
Cleanroom Regulations, Classifications, Basic Background and Design Considerations
Cleanroom Qualification, Cleaning Validation (IOQ/PQ), Routine Monitoring and Excursion Investigation
Environmental Monitoring Program (Monitoring, Excursion Investigation and Trending of Data)
Personnel Training (Aseptic Practices, Cleanroom Behavior and Contamination Control Procedures)
Cleanroom Trafficking (Cleanroom Personnel Material, Product and Equipment Transfer Practices and Training (Entry and Exit Policy)
Cleanroom Gowning, Contamination Control, Cleaning and Disinfection Program
Basics of Sterilization Processes- Physical and Chemical Processes
Bonus:Compliance Expectations, FDA Form 483’s and Case Studies
In-Person Seminar going Virtual with increased learner satisfaction.
Yes, attend this seminar from anywhere. We are making it real and more interactive – Here's a sneak peek:
Our enhanced delivery process and technology provides you an immersive experience and will allow you to access:
The real-time and live presentation as in in-person events
Private chat for company-specific conversation – the same as you would get in an in-person seminar
Opportunities to connect with your peers to share knowledge at a different time and have group discussions
Live workshop activities
Live Q&A during the event and offline Q&A assistance after the event
As usual more content, activities and case studies and now adding homework for a comprehensive understanding
Certification
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