$150.00

Medical Devices for Risk Management Techniques 2017

Risk Management Techniques for Medical Devices

Description

Overview:
This course will help you understand the regulatory requirements, including

ISO14971, and how to create processes and procedures to implement them.

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.

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
Stages of Risk Management as well as Tools and Techniques
Judging the probability that harm may occur from those hazards

Who Will Benefit:
Design Engineer
Manufacturing Engineer
Quality Engineer
R&D Personnel
R&D Project Managers
Quality Managers
Auditors
Regulatory Affairs Specialist
R&D Manager

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.

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

Ad Reference ID: 1405940d8989df20

Report problem

Processing your request, Please wait....

Leave a Reply

*

To inquire about this ad listing, complete the form below to send a message to the ad poster.