This webinar will cover the latest trends and regulatory expectations in the industry for disinfectant validation studies.
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Current Industry Best Practices in Disinfectant Validation
Designing an effective disinfectant validation program to meet FDA, MHRA, HPRA, EMA scrutiny. This webinar provides guidance on industry trends, regulatory feedback, and designs for an effective validation program. Current 483's, Warning Letters, European Regulations, and Field Experiences as well as case studies will be conveyed that allow end users to determine that best methods to validate their products against their environmental isolates. Current industry best practices will be covered as well as potential pitfalls that can occur during testing.
Why should you attend: The topic of suspension and coupon studies will be discussed as well as possible errors that can happen with the testing.
The FDA and other industry regulators have an expectation that disinfectants, sanitizers, and sporicides used in cleanrooms will need to be validated which has created an increased interest in coupon testing.
Areas Covered in the Session:
Who Will Benefit:
- 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.
- Quality Managers
- Regulatory Affairs
- 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