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

MessageThis Webinar is over
Date Nov 15, 2018
Time 10:00 AM to 11:30 AM
Cost 150.00
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 

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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