Ensuring Medical Devices are safe and [Effective] for Intended Uses

  • 150.00 Dollar US$
  • Published date: September 12, 2018
    • Fremont, California, United States

Overview:
You'll learn techniques that can help you identify hazards and potential

harms. You'll learn how to mitigate risk and effectively monitor risk to

ensure your customers receive safe and effective products.

Why should you Attend:
Many companies have even experienced class action law suits because of

product quality issues. An effective program of risk management can help

you proactively identify and mitigate product risks. A good risk

management process can help you methodically identify, mitigate, and

monitor risk throughout the product life-cycle.

Areas Covered in the Session:
Overview of the ISO14971 standard as it applies to medical device

companies.
Integrating the new standard with ISO 13485 as part of your overall QMS
Conducting a review of the intended use of your device.

Who Will Benefit:
Design Engineer
Manufacturing Engineer
Quality Engineer
R&D Personnel

Speaker Profile:
Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the

medical device industry with emphasis on quality, compliance, and six

sigma. She has an extensive background in quality and compliance for

medical devices from new product development, to operations, to post-

market activities.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com

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Compliance4All
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