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FDAnews Announces — Medical Device Risk Management: From Understanding to Applications, Nov. 5-6, 2014
Date:8/25/2014

ing one apart to make it better.

Who Will Benefit:

  •     Project managers involved in design and development
  •     Design engineers
  •     Quality engineers
  •     Manufacturing engineers
  •     Quality auditors
  •     Production managers
  •     Scientists involved in device research and development
  •     Medical staff evaluating risk, safety or effectiveness
  •     Quality or regulatory staff assigned to complaint, CAPA or MDR management
  •     Training personnel
  •     General/corporate counsel

Meet the Instructor:
Dan O’Leary has more than 30 years’ experience in quality, operations and program management in regulated industries including, aviation, defense, medical devices and clinical labs. Dan is now President of Ombu Enterprises, LLC, a consultancy focused on operational excellence and regulatory compliance serving small manufacturing companies. He has a Masters Degree in Mathematics; is an ASQ Certified Biomedical Auditor, Quality Auditor, Quality Engineer, Reliability Engineer and Six Sigma Black Belt; and is certified by APICS in Resource Management.

Conference Details:
Medical Device Risk Management:
From Understanding to Applications
**Presented by Ombu Enterprises and FDAnews**
Nov. 5-6, 2014 — Schaumburg, IL (Chicago)
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