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How to Develop the Risk Management File - 2017

 
  August 09, 2017  
     
 
Netzealous LLC DBA - Compliance4All, Online
2017-10-18


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



Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support@compliance4All.com
 
 
Organized by: Event Manager
Invited Speakers:
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.
 
Deadline for Abstracts: 2017-10-17
 
Registration:
Full Details & Registration Link:
 
E-mail: support@compliance4All.com
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