FDA Compliance 2012 - Understanding Disinfectant Qualification Studies ? How to Avoid Errors
Date2012-03-01
Deadline2012-03-01
VenuePalo Alto, USA - United States
KeywordsDisinfectant Qualification Studies; Disinfectant Validation; Regulatory requirements for disinfectants; disinfectant testing methodologies
Topics/Call fo Papers
This 90-minute webinar on Disinfectant Qualification Studies will teach you disinfectant testing methodologies, provide examples of disinfectant efficacy tests and show how to troubleshoot problems related to disinfectant efficacy testing.
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.
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- Prepare for Tougher U.S. FDA cGMP Compliance Audits
- Verification and Validation Planning Under U.S. FDA cGMP, ICH Q9 and ISO 14971
- Major CGMP Issues for 2012 - Webinar by ComplianceOnline
Last modified: 2011-12-26 17:52:26