The Human Factor’s Engineering Process in the Development of Medical Device Software
08/27/2010

Edmond Israelski
| medical devices
| medical devices
| medical device software
| software design
| design control process
| HFE medical devices
| human factors engineering
|
|
View this presentation to find out about integrating human factors engineering into medical devices to make them safe, effective and efficient to use, and the regulations for the human factors engineering process.
Presented by Dr. Edmond W. Israelski, Human Factors Program Manager, Abbott Laboratories, at IQPC's 12th Software Design for Medical Devices conference in 2009.
-
Delivering and Sustaining Lean on the Shopfloor -
Treating Asthma with Monoclonal Antibody Based Drugs: Past Experience and Future Prospects -
Assessing the Global Impact of Standardisation on Manufacturers: Is it Really Worth it? -
Reviewing Recent European Cases to Implement Best Practice Patent Filing Strategies for the Future -
Dealing with Changes in the Marketplace: Mergers and Acquisitions in the CRO Industry and their Impact on Sponsors -
Crystalline Forms –The Next Generation -
U.S. Judicial Decisions Impacting Co-Crystal Patent Strategy -
Crystallisation: The Broad Perspective -
Pharmaceutical Cocrystals: Positive Effects on Drug Properties -
F. Hoffman La-Roche Case Study: Spearheading the Global Roll-Out of a Global E-mail Management and Retention Project
You Should Check Out:
* = required.
Not a member yet? Sign up
Events of Interest
-
Software Design for Medical Devices
The HUB Commerce Square, Philadelphia, PA
May 21- 23, 2012 -
Business Process Excellence for Pharmaceuticals, Biotech and Medical Devices
Guoman Charing Cross, London, UK
April 25- 27, 2012 -
International Conference PLM in Pharmaceutical & Biotechnical Development
Dorint Hotel Sanssouci Berlin-Potsdam
May 21- 23, 2012 -
Information Governance & eDiscovery for Pharma, Biotech and Medical Devices
London, UK
June 26- 28, 2012
You Might Also Like
-
Software Design for Medical Devices
Software is playing an increasing role within the development of medical devices and the pharmaceutical... Read more
Pharma IQ
-
What's Next for the Medical Devices Market? Regulatory Changes
With the increasing evidence-based medicine politics, the medical device market is changing. In this
Pharma IQ
-
Medical Devices: Directives and Standards
The term medical devices covers a wide range of products, from simple tongue depressors to highly complex... Read more
Pharma IQ
-
Keeping a Pace with Changes in Clinical Evaluations for Medical Devices
Danielle Giroud, Founder of the World Medical Device Organisation, joins Pharma IQ to discuss regulatory... Read more
Helen Winsor






Not a member? Sign Up
Reasons for Joining
Address your challenges through knowledge sharing with peers from our global network of specialists.
Benchmark your business initiatives with the who's who in the field.
Hear from industry pioneers how to maximize ROI in today's challenging economy.
And best of all It's FREE!