Sterility is both a critical quality attribute and one that is most difficult to consistently demonstrate to regulators in parenteral products. Join our expert during his upcoming webinar hosted in collaboration with the Executive Conference Corporation to get an in-depth look at the most common myths related to key sterility assurance programs, to ensure qualified environments remain in a state of microbiological control.
The following myths will be dispelled during the webinar:
Disinfectant Quantity - the misconception that more disinfecting agent is always better for sanitization of surfaces
Microbiological Resistance - the misconception that microorganisms will develop resistance over time to the use of disinfectants
Disinfection Rotation - the misconception that disinfection rotation is required to prevent microbiological resistance
Effectiveness of Isopropyl Alcohol - the misconception that 70% Isopropyl Alcohol (IPA) is effective for control of fungal and bacterial spores.
Who Should Attend? Validation Managers, Quality Control Managers, Quality Assurance Managers, Lean Managers, Operations Managers, Cleanroom Managers, Regulatory Affairs Managers, Production Managers