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Upcoming Webinar on Medical Device Software Development Compliance

3-hr Virtual Seminar: Outsourcing Medical Device Software Development with Compliance to IEC 62304

Medical Device software must be developed under an IEC 62304 software development process since March of this year. It is critical to understand IEC 62304 well enough to ensure compliance by the vendor and that the deliverables meet the IEC 62304 requirements.

If you have software written for medical devices by an outside company, you should attend this webinar:

  • Software quality assurance managers and engineers
  • Quality Assurance managers
  • Product engineering managers
  • Product program managers
  • Product development project managers

Attend Live Online Training
November 02, Wednesday 09:00 AM PDT | 12:00 PM EDT

Register at http://www.complianceonline.com/ecommerce/control/trainingFocus?product_id=702133&category_id=10002&full_desc=yes

Instructors:

  • Tim Stein, President and CEO of Business Performance Associates, Inc.,
  • Walt Maclay, President of Voler Systems

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Voler is really good at identifying risks and finding the best way to do a project on-time, on spec, and easy to manufacture.