MD&M West: 20 Collocated Conferences Under One Roof

The premier conference programs for research and development, design, engineering, quality, manufacturing, and regulatory affairs professionals within the medical device industry

Last chance to register! Conference sessions start Monday, February 13th. Register now to join hundreds of your peers to gain must-have knowledge for 2012.

Find new ideas and insights from 120 industry experts at the MD&M West Conference. With 20 full-day conference programs, we offer customizable programs to get you the timely solutions you need to develop your next-generation medical products within a robust quality management system.

Find the most relevant solutions for your job. View our featured conference programs or scan the full agenda below!

Conference Full Agenda Monday, February 13 Session 100 Crafting Approvable Submissions for Today's Challenging Regulatory Environment – Experts' Tips for Success Session 101 Process Validation: Solutions and Strategies for the Medical Device Industry Session 102 Adapting to a New Era of Supplier Controls Session 103 Adhering to New Human Factors Requirements Session 104 Advances in Medical Polymers for Medical Devices Sponsored by: Tuesday, February 14 Session 200 Morning: CDRH Top Headquarter Officials Discuss Product Clearances and Quality System Compliance for 2012 Afternoon: Activities in the FDA's LA District Session 201 Integrating Design Control Principles into Process Validation Session 202 Risk Management for Medical Devices: Applying 14971 Effectively Using Risk Assessment and Reliability Tools Session 203 Creativity within Constraints: How to Move from Good to Great Design Session 204 New Materials Processing Technologies for Medical Devices Wednesday, February 15 Session 300 Morning: Revelations of Former FDA and Department of Justice Officials Afternoon: Gearing Up For Complying with FDA and International Regulatory Requirements Session 301 Applying Product Design Tools Session 302 Beyond Basic Risk Management: How Much is Enough? Session 303 Product Development and FDA Approval Process for Medical Devices Session 304 Medical Devices with Batteries Thursday, February 16 Session 400 Morning: Balancing Risk and Reward in Your Product Portfolio Afternoon: Product Disasters and Multifunctional Response Strategies Session 401 Product Life Cycle Management Session 402 Creating a Global Quality Management System Session 403 Medical Device Reliability Testing Session 404 The A,B,C's of Product Sterilization Selection

Exclusive Lunch & Learn Presentation - Tuesday, February 14 Join Nelson Laboratories for a special presentation on recent FDA trends impacting in vitro hemocompatibility and genotoxicity testing. Call 310-996-9435 for details.

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Featured Speaker Interviews

Richard Meyst
President & CEO
Fallbrook Engineering, Inc.

Dhuanne Dodrill
President
Rollprint Packaging Products, Inc.

Isidor Buchmann
CEO & Founder
Cadex Electronics Inc.

Conference Sponsors

For conference sponsorship
opportunities, contact:
Christine Nguyen at 310-996-9445
or christine.nguyen@ubm.com