Browse Categories

Search By
Category
Speakers
Month

 Speaker Profile


Edwin L Bills
Principal Consultant, Bilanx Consulting LLC

During his 20 year career in medical devices, Mr. Bills has held a number of quality and regulatory affairs positions. Mr. Bills is ASQ Certified as Quality Engineer, Quality Auditor, and as Manager of Quality/ Organizational Improvement. He also holds a certificate as Regulatory Affairs Certified through the Regulatory Affairs Professionals Society, and a BS and Masters degree from the University of Cincinnati. Recently, Mr. Bills served as US Industry Co-chair of the Association for Advancement of Medical Instrumentation committee, QM/WG04, on application of risk management to medical devices and is a current member of this group. Mr. Bills has presented at training courses for the American Association of Medical Instrumentation (AAMI) in the area of risk management and quality systems. Currently, Mr. Bills is the Principal Consultant at Bilanx Consulting LLC in the area of medical device quality, regulatory, product liability and risk management.

 Upcoming Webinars
Use of Risk Management to Meet Requirements of IEC 60601-1
This presentation will examine the requirements of IEC 60601-1 for use of ISO 14971 risk management and interpret those requirements.
Live  Thursday, August 26, 2010 10:00 AM PDT | 01:00 PM EDT,  Duration:90 Minutes
$245.00

Post-Design Medical Device Risk Management
In this presentation we will explore the requirements for post-design risk management and determine how to apply the requirements.
Live  Tuesday, September 7, 2010 10:00 AM PDT | 01:00 PM EDT,  Duration:90 Minutes
$245.00

Why Medical Device Companies Receive Warning Letters
The Commissioner of the US FDA has stated the agency will be more enforcement oriented and quicker to issue Warning Letters. This presentation will review current enforcement practices of the US FDA with actual Warning Letters recently issued to medical d
Live  Tuesday, September 21, 2010 10:00 AM PDT | 01:00 PM EDT,  Duration:90 Minutes
$245.00
...more
 Recorded Webinars
How does Risk Management Impact Supply Management
This course will demonstrate how to use risk management tools effectively to select suppliers that impact safety and to communicate to suppliers where they need to apply special attention to reduce the risk of their products to the medical device manufact
Recorded ,
$295.00

Use of Risk Management during Process and Design Validation
This presentation will discuss this critical interface between these three elements and give medical device manufacturers practical advice on implementation of a process that meets the requirements of all three areas.
Recorded ,
$295.00

Proper Documentation of Risk Management for Compliance with ISO 14971
This presentation will deliver a practical discussion on the proper use of the tools available to conduct product risk management and achieve a result that complies and also provides a more complete product risk analysis resulting in reduced cost and impr
Recorded ,
$295.00

Integrating Risk Management Into the Quality System
ISO 14971 medical device risk management standard was updated in 2007 after its initial release in 2000.
Recorded ,
$295.00

...more


About US | FAQ | Support | Contact Us | Feedback | Terms & Conditions | Privacy Policy | Legal Disclaimer | Unsubscribe
All rights are reserved © GlobalCompliancePanel.