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 and Presenter Information
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.
Relevant Government Agencies
Risk Management
Event Type
Webcast
This event has no exhibitor/sponsor opportunities
When
Wed, Oct 18, 2017, 10:00am - 11:30am
PT
Cost
Live Webinar: | $150.00 |
Recorded Webinar: | $190.00 |
Website
Click here to visit event website
Organizer
NetZealous - Compliance4All