How to Investigate Environmental Monitoring Excursions

This OOS investigation training will review the various items that should be included in the investigation to determine the cause of the limit excursion for both viable and non-viable excursions.

Why Should You Attend:

Medical products are manufactured in environments that control the level of viable and non-viable particulate and to establish that the control is taking place periodic monitoring must be performed. But any time monitoring occurs there is the potential that the results will exceed limits that have been established.

Who Will Benefit:

This webinar will provide valuable information to all companies that manufacture medical products in environments that are controlled and monitored for viable or non-viable contamination.

QA personnel

Manufacturing

R&D

Instructor Profile:

Gerry O'Dell, is president of Gerry O’Dell Consulting, a consulting firm based in the United States with clients around the world. Ms. O’Dell consults to medical device and pharmaceutical companies on all the major sterilization methodologies, microbiology, environmental control, laboratory compliance, failure investigation, etc. Her varied background includes extensive knowledge in sterilization technology, laboratory management, microbiological testing (including pyrogens), decontamination of returned goods, and compliance.

Note:

Use coupon code NB5SQH8N and get 10% off on registration.

For Registration:

http://www.complianceonline.com/failure-or-oos-investigation-for-environmental-monitoring-viable-and-nonviable-webinar-training-701354-prdw?channel=sciencedz