The safe transfer of materials into a controlled area is one of the greatest challenges of managing cleanrooms and isolators. New regulations, for example the recent update of EU GMP Annex 1, put a stronger emphasis on the strict control and understanding of this process.
In this webinar, we will look at some of the environmental monitoring aspects to consider when materials need to be transferred into controlled areas, and how some recent improvements can assist you in this task:
- Culture media handling: How culture media such as the ICR plates for isolators and cleanrooms can easily be introduced into a controlled area.
- Transfer of product into isolators: How rapid transfer solutions can help you become more flexible while minimizing the contamination risk for your isolator campaigns.
- Consumables handling: How the new Safe Lid for the MAS-100® range of samplers can simplify your air monitoring.
Speakers
Kristian Siedler
Merck
Global Product Manager
Kristian Siedler is the Global Product Manager in charge of the portfolio of specialized culture media for use in isolators and cleanrooms. He is responsible for the continuous development and success of the portfolio as well as for global troubleshooting. In his almost 10 years in various sales and product management positions within the industry, he has been able to gather firsthand experience on the regulation, use and handling of these products.
Dr. Anne-Grit Klees
Merck
Global Product Manager Environmental Monitoring
Dr. Anne-Grit Klees is responsible for Innovation & Product Life Cycle Management with regard to microbial air samplers and media for aseptic process simulation for pharma cleanrooms and isolators. With a professional background in microbiology, she has been working in product and marketing management within the health industry for 30 years.
Microbiological testing
- Viable air monitoring
Duration:1h
Language:English
Session 1:presented July 11, 2024
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