Troubleshooting Ethylene Oxide (EO) Processes

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Category FDA GXP Compliance - Medical Devices

Deadline: April 07, 2015 | Date: April 07, 2015

Venue/Country: Palo Alto, U.S.A

Updated: 2015-03-31 20:09:26 (GMT+9)

Call For Papers - CFP

Why Should You Attend:

Ethylene oxide (EO) sterilization is the most complicated of the industrial sterilization methods. It is not uncommon for anomalies to occur during qualification or routine processing. These anomalies may come in the form of sterilization cycle parameter that is not achieved or a positive biological indicator.

Who Will Benefit:

This webinar will provide valuable information to all companies that produce sterile products.

QA personnel

Validation specialists

Manufacturing personnel involved in validations

R&D specialists

Instructor Profile:

Gerry O’Dell, is owner and President of Gerry O'Dell Consulting, a consulting firm based in the United States with medical device and pharmaceutical clients around the world. Gerry O'Dell Consulting works to assist companies to comply with requirements to assure that their product is sterile at all stages of the development and manufacturing process.

Note:

Use coupon code 232082 and get 10% off on registration.

For Registration:

http://www.complianceonline.com/troubleshooting-ethylene-oxide-eo-processes-for-medical-device-sterilization-webinar-training-701679-prdw?channel=ourglocal