How to Develop the Risk Management File - 2017

Fremont (United States), 18 October 2017


Key deadlines
Conference starts:
2017-10-18
Website

Visit the conference website

Conference Description

Overview:
The single most important element of medical device risk management is the Risk Management Plan (RMP). It ranges from Top Management's risk policy to review and approval of the Risk Management Report. Get these items wrong and the rest of your risk management process will suffer.

Why should you Attend:
This presentation gives you the essential information you need to write a successful plan. Many companies try to implement Risk Management using an inadequate Risk Management Plan. They often leave out required items or add additional, but unnecessary information.

Who Will Benefit:
Risk Managers
Project Managers
Risk Management Team Members
Design Project Team Members
Complaint Specialists
MDR Specialists

Speaker Profile:
Dan is the President of Ombu Enterprises, LLC, a company offering training and execution in Operational Excellence, focused on analytic skills and a systems approach to operations management. Dan has more than 30 years experience in quality, operations, and program management in regulated industries including aviation, defense, medical devices, and clinical labs.

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

Conference creator: compliance4all

Actions menu

Conference Location

image placeholder

18004479407 161 Mission Falls Lane, Suite 216,
Fremont 94539 (United States)

Tags for this conference

Comments

No comments yet!

You must register or sign in to post a comment.