Medical Device Manufacturing Conference

Selecting and working with contract manufacturers,integration of compliance and regulatory standards,and creating a scaleable manufacturing operation

March 3-4, 2008
Houston, TX

Over the course of the past 20 years, the Medical Device industry has experienced tremendous growth and increased product complexity due to the availability and use of enhanced product materials and technology imbedded within medical device products.  Many of these innovations have been driven by manufacturing capabilities and the opportunities for the use of highly durable, long-lasting products.  In an industry where even the slightest manufacturing malfunction or error can result in disastrous repercussions for users, assuring constant product quality is of primary concern for executives within manufacturing divisions.  Adding to this the ever increasing regulatory presence along with the constant requirement of reducing costs has resulted in an environment of immense strain.

Sessions and Speakers Include:

FDA Reporting Practices: When, What and Why?
Casper E. Uldriks, JD, MDiv.
Associate Director for Regulatory Guidance and Government Affairs
Office of the Center Director CDRH / FDA

International Manufacturing: Devices Move Abroad
Corinne Lyle
CVP Global Operations
Edwards Lifesciences

Selecting the Partners to Facilitate the Manufacturing of Your Device
Roger Talish
Founder, COO, VP of Engineering
Juvent Medical

Future Environmental Directives for Medical Device Industry
Dr. Ronald Lasky
Senior Technologist
Indium Corporation
* 2nd Day Conference Chair Person

Click Here to Read Dr. Lasky's Blog

And More...

For Additional Details on this Program:
Paul Hernandez, Marketing Manager
PHernandez@Q1productions.com
312-602-9684