What to identify? Why Screening Cleanroom Microbes Matters

Duration: 60 Minutes
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This webinar will look at microbial identification for pharmaceutical and healthcare facilities, examining the common types of organisms isolated from pharmaceutical cleanrooms; the methods of identification; and the inferences that can be drawn from identification patterns; how often to identify and when to identify; ways to trend cleanroom microorganisms; the level of detail that can be assessed from genotypic and phenotypic identification; and the uses of isolates in terms of the testing of culture media, use in microbial validation; and for disinfectant efficacy testing.
Validating and Monitoring the Cleanroom
Instructor: Tim Sandle
Product ID: 506386
Objectives of the Presentation
  • Common types of microorganisms from pharmaceutical and healthcare cleanrooms
  • Identification strategy
  • What variances in trend signify, e.g. a shift in spore-forming organisms
  • Actions to take for out-of-trend situations
  • Methods for trending
  • Differences between identification technologies
  • Different types of culture media
Why Should you Attend
To review baseline data relating to cleanroom isolates (there are very few referenced studies); to consider ways to trend data; and to consider the range of uses to which isolates can be put within the microbiological laboratory. This will include when to use environmental isolates and how often.

Areas Covered
  • Cleanroom microbial trends
  • Phenotypic identification techniques
  • Genotypic identification techniques
  • How to trend data
  • How to draw inferences from data
  • How to select environmental isolates
  • The pros and cons of using environmental isolates
  • How often to rotate environmental isolates
Who will Benefit
  • Pharmaceuticals
  • Healthcare
  • Medical devices
  • Cleanrooms
  • Biotechnology
  • Academia
Topic Background
The typical microbiology laboratory is faced with hundreds of samples for identification. This creates a dilemma: how often to identify? What to identify? Which methods should be used? And how can the data be interpreted? This webinar addresses these questions and provides guidance. The webinar also considers the use to which representative isolates from cleanrooms can be put, in terms of culture media testing, microbial validation, and disinfectant efficacy testing.
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  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
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  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Dr. Sandle has over twenty-five years experience of microbiological research and biopharmaceutical processing. He is Head of Microbiology at Bio Products Laboratory (U.K.) and a visiting tutor with The University of Manchester School of Pharmacy. Dr. Sandle serves on several national and international committees relating to pharmaceutical microbiology and cleanroom contamination control. He is a committee member of the Pharmaceutical Microbiology Interest Group (Pharmig); and is a member of several editorials boards for scientific journals.

Dr. Sandle has written over three hundred book chapters, peer reviewed papers and technical articles relating to microbiology. Dr. Sandle's current research interests are cleanroom fungi; microbiology of water; disinfectants; and rapid microbiological methods.

In addition, Dr. Sandle serves on several national and international committees relating to pharmaceutical microbiology and cleanroom contamination control (including the ISO cleanroom standards). He is a committee member of the Pharmaceutical Microbiology Interest Group (Pharmig); serves on the National Blood Service advisory cleaning and disinfection committee; and is a member of eleven editorials boards for scientific journals.

Dr. Sandle has acted as a consultant, expert witness and technical advisor to sterile and non-sterile manufacturing facilities, microbiology laboratories, the medical device industry and hospitals. Dr. Sandle has also undertaken several technical writing and review projects.
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