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

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