Designing an Effective Cleaning Validation in today's Regulatory Environment - Webinar By GlobalCompliancePanel

FOR IMMEDIATE RELEASE
(Free-Press-Release.com) August 28, 2011 --

Why you should attend: We've all seen headlines about so-&-so company having to recall such-&-such product due to safety concerns. The worst of these stories detail injury and death of patients. In many of these situations, product contamination is at the center of the issue. Contamination of medical products, whether they are devices, drugs, or diagnostics, can be controlled and eliminated based upon sound cleaning validation studies. These studies can often be complex and intimidating. Yet, with experience and careful design, effective cleaning validation can protect patients and ensure your company's compliance with regulatory expectations.

Areas Covered in the Session:
What are FDA Requirements and Industry Standard Practices
What are the steps to follow?
What preparatory work is needed before starting validation?
What are documentation requirements?
Cleaning Validation Maintenance – How to remain under a validated status
Who Will Benefit:
QA managers and personnel
Regulatory affairs
Operations managers
Engineers
Validation professionals
Training departments
Consultants
Quality Engineers

Cleaning Validation Maintenanc     documentation requirements     FDA requirements     Regulatory Environment