How to Develop the Risk Management File - 2017

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
At a Glance
When 18 October 2017
Where Fremont, CA, United States
Organizer Netzealous LLC DBA - Compliance4All
Event Type conference
Official Website
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Added by Compliance4all
Added on 09 August 2017
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