Email this Page
Print this Page
   How Manufacturers Can Reduce End-of-Line Testing

By using advanced process monitoring technologies, medical device manufacturers can reduce their need to conduct expensive and time-consuming end-of-line testing on finished medical products. This FREE Webinar reviews current trends in medical product testing, including the use of process signature analysis to establish the ultimate level of process control. Adoption of process signature analysis supports the FDA initiative for process analytical technology (PAT) and can improve process control, reduce waste, increase yields, and reduce costs.
Web Event: How Manufacturers Can Reduce End-of-Line Testing
Date:

Thursday,
September 14
Time: 2:00 EDT (1:00 CDT, 11:00 PDT)
Duration: 50 minutes
Who should attend: Technical and management personnel involved in process monitoring and process control.
   TO REGISTER
   CLICK HERE

“How Manufacturers Can Reduce End-of-Line Testing” will feature three live presentations by industry experts with extensive experience in the field of signature analysis and process monitoring. Panelists for the Webinar include:

Supporting FDA’s PAT Initiative
Tom Hayes
General Manager of ATS Compliance Solutions
ATS Test Systems
Current Functional Test Techniques
Drew Wilson
Director of Technology and Business Development
ATS Test Systems

Signature Analysis: Applying Science to Manufacturing
Laura Dierker
Marketing Manager for Life Sciences
Sciemetic Instruments
   
The Webinar will conclude with a live Q&A session moderated by Sherrie Conroy, editor-in-chief of MD&DI magazine.

TO REGISTER FOR THIS EVENT CLICK HERE
   
Sponsored By:

 
©2006 Canon Communications LLC

Canon Communications LLC
11444 W. Olympic Blvd.
Los Angeles, CA 90064