Attend the Orthopaedic Industry’s Leading Technology Conference

With the increasing cost pressures from hospitals and the higher level of scrutiny from FDA, you need to be on top of your game when it comes to streamlining and implementing efficient, lean product design processes.

Can you confidently answer these questions?

  • What’s happening now and next?
  • What are the new materials and technologies in development?
  • Have they been successful in the market? And more importantly, are they effective?
  • What are the best methods of analyzing these technologies?

Spend two days learning and networking with 400 orthopaedic manufacturing professionals.
Conference Agenda • New Training Workshops • Speakers
Register now or call 310-996-9435 for questions or more details.


Attend OrthoTec 2012 and gain the answers you need with presentations targeted specifically towards today’s orthopaedic technology professional. A mix of experts from academia, manufacturing (OEMs and suppliers), and the regulatory field presenting at the OrthoTec conference will provide updates, share insights and discuss best practices. The conference is the ideal opportunity to network with over 400 of your industry peers at industry’s largest annual gathering of R&D, design, engineering, and quality professionals within the orthopaedic manufacturing sector.

This year’s timely OrthoTec panels include:

  • New Materials Technology and Applications
  • Applying New Technologies in Surfaces
  • Creating Robust Processes to Enable Better Design
  • New Design Tools and Technologies

New at OrthoTec: Two In-Depth Training Workshops!


Receive high quality training on two of the most important aspects of orthopaedic product development for only $249 for each three-hour workshop. Space is limited to thirty-five delegates each day. Call 310-996-9435 for more information.

Validating Manufacturing Processes, June 6, 2012
Is your company aware that it may need to validate some or all of its manufacturing processes, but not quite sure how to get started? Gain the knowledge to help jumpstart your validation programs and put yourself in a defendable position with the regulatory bodies. This presentation is broken up into four main discussion areas in order to provide a systematic approach validating your manufacturing processes.

Risk Management – Getting Control of the ‘What Ifs’, June 7, 2012
There are threads of risk management throughout the regulations in such areas as CAPA, process validation and design controls. Assess your basic understanding of risk and build the knowledge needed to conduct your own risk assessment.