Tuesday September 28, 2021
12:00 Noon – 1:00 pm EDT
Instructor: Jim Polarine
Sterility is one of the most critical quality attributes that all parenteral products must possess; yet, it is one of the most difficult to consistently demonstrate to regulators. This presentation will discuss four (4) of the most common myths related to one of key sterility assurance programs to ensure qualified environments remain in a state of microbiological control. This session will be an effort to dispel many of the myths that still exist in the cleanroom today:
- 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 myth that multiple disinfectants are needed for a rotational program.
- Effectiveness of Isopropyl Alcohol – The misconception that 70% Isopropyl Alcohol (IPA) is effective for control of fungal and bacterial spores.
These four myths will be de-mystified throughout the sessions through good science, technical expertise and case studies. The attendees will understand the importance of developing a robust sanitization along with clear understanding of these myths to develop a risk-based sanitization program for current and future technologies.
Who Should Attend the Webinar:
- Validation Managers
- Quality Control Managers
- Quality Assurance Managers
- Lean Managers
- Operations Managers
- Cleanroom Managers
- Regulatory Affairs Managers
- Production Managers
Fee:
$385 for one person
$700 2-5 people
$999 6-10 people
Questions? support@eccwebinars.com
ECC-335