Biological Contamination Events In Isolators: What Lessons Can Be Learned?
By James Drinkwater, Bioquell UK Process & Compliance Director
Microbiological deviation and biological contamination events have been observed in pharmaceutical isolators including those used in production, sterility test and pharmacy aseptic services. This paper considers a range of ‘real-life’ biological contamination event cases studies, reviews the root causes that were identified and looks at what lessons can be learned.
access the White Paper!
Log In
Get unlimited access to:
Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue.
X
Enter your credentials below to log in. Not yet a member of Bioprocess Online? Subscribe today.
Subscribe to Bioprocess Online
X
Subscribe to Bioprocess Online
This website uses cookies to ensure you get the best experience on our website. Learn more