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Understanding Disinfectant Qualification Studies – How to avoid errors

 
  October 30, 2012  
     
 
ComplianceOnline, Online Event
2013-03-08


Why Should You Attend:

How do you design an effective disinfectant validation program that meets FDA , MHRA, EMA scrutiny?

This webinar provides guidance on industry trends, regulatory feedback, and designs for an effective validation program. Current 483's, Warning Letters, and Field Experiences will be conveyed that allow end users to determine the best methods to validate their products against their isolates.

Areas Covered in the Seminar:

  • Learn disinfectant testing methodologies.
  • Review “real world” examples of disinfectant efficacy tests.
  • Increase awareness of pitfalls encountered during testing.
  • Troubleshooting problems related to disinfectant efficacy testing.
  • Examples of disinfectant validation successes will be discussed.

Who Will Benefit:

This webinar will provide valuable assistance to all FDA and EMEA regulated companies that need to validate their cleaning and disinfection programs, including companies in the Pharmaceutical, Biotech, and Medical Device fields. The employees who will benefit include:

  • QA and QC Managers
  • Disinfectant Validation Managers
  • Operations Managers
  • Cleanroom Managers
  • Personnel and contractors that clean and disinfect cleanrooms
  • EH&S Managers
  • Regulatory Compliance Managers & Environmental Monitoring Managers
 
 
Organized by: Complianceonline
Invited Speakers: Mr. Polarine, is a technical service manager at STERIS Corporation. He has been with STERIS Corporation for over eleven years, where his current technical focus is microbial control in cleanrooms and other critical environments. He has lectured in North America, Europe, Asia, Latin America, and Puerto Rico on issues related to cleaning and disinfection in cleanrooms. Mr. Polarine is a frequent industry speaker and has worked on several books and article publications related to cleaning and disinfection and contamination control. He is currently co-authoring several articles and is a co-author on the PDA technical report on cleaning and disinfection. He is also currently active on the PDA task force on cleaning and disinfection.
 
Deadline for Abstracts: 2013-03-07
 
Registration:

For Registration:

http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702210?channel=hummolgen 

E-mail: referral@complianceonline.com
 
   
 
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