April 04th, 1:00 PM – 2:00 PM EDT
If prevention of microorganism contamination applies to your business, then we have the right module for you in this webinar.
This session will review the corrective and preventive action FDA procedure involving the use of specialized equipment in a clean room. Understand;
- The definition of Aseptic processing
- Terminal Sterilization vs. AP
- Facility design and how it impacts the product
- Proper environmental monitoring
Why Should You Attend:
This environmental control in pharmaceutical industry webinar is a good refresher for those personnel that are familiar with the way to properly work in the clean room and why environmental control rooms are designed for proper contamination control.
Areas Covered In This Webinar:
In sterile compounding, aseptic technique is contributing to the prevention of microbiological contamination. It is providing sterility, safety, and efficacy to the sterile product, especially various injections for patients.
Cleaning, Gowning and proper methods of contamination control will be reviewed keeping in mind FDA audit training, FDA CGMP compliance and FDA environmental monitoring, along with why clean rooms are designed the way they are.
Instructor Danielle DeLucy, is the owner of ASA Training and Consulting, which provides Pharmaceutical and Biologics companies with assistance to meet regulatory compliance.
At AtoZ Compliance, we focus on our core values – quality, expertise, and customer experience which are the foundation of our business. We take extreme care in selecting topics which are highly relevant to you.