Biotech Webinar 2011 - Solutions for addressing microbial excursions in medical device, pharmaceutical, and biotech industries
Date2011-01-07
Deadline2011-01-07
VenuePalo Alto, USA - United States
KeywordsBiotech,conference,event,Webinar
Topics/Call fo Papers
Why Should You Attend:
The most common sources for microbial excursion are personnel practices, cleaning and disinfection program, facility design and conditions, and bringing items into the clean room. This webinar will discuss the details of specific excursion investigation for outbreaks of molds, vegetative bacteria, and Bacillus. End users will gain a new understanding of the complexity of troubleshooting outbreaks and contamination issues based on real life experiences.
Case Studies will be discussed and reviewed involving bacterial and fungal outbreaks in clean room operations. Contamination Control strategies will be reviewed and discussed in detail. Real world scenarios will be discussed from best practices in contamination control perspective.
The most common sources for microbial excursion are personnel practices, cleaning and disinfection program, facility design and conditions, and bringing items into the clean room. This webinar will discuss the details of specific excursion investigation for outbreaks of molds, vegetative bacteria, and Bacillus. End users will gain a new understanding of the complexity of troubleshooting outbreaks and contamination issues based on real life experiences.
Case Studies will be discussed and reviewed involving bacterial and fungal outbreaks in clean room operations. Contamination Control strategies will be reviewed and discussed in detail. Real world scenarios will be discussed from best practices in contamination control perspective.
Other CFPs
- Clinical Trial auditing - Identifying risks and building a more compliant and successful trial
- Trial Master File for Research Sites: Can You Pass FDA Inspection? - Webinar By ComplianceOnline
- How to Vet an IRB: Expose and Fix Problems Before They Threaten Your Trial
- Design Validation Protocol and Acceptance Criteria for Chromatographic Methods to meet ICH requirements
- Eliminate the Confusion ?Annex 13 GMP guide - Webinar By ComplianceOnline
Last modified: 2010-12-23 19:58:15