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We’re Only Human: Addressing Human Imperfections and Variability in Standards Work
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Please join our speaker Molly Follette Story, PhD, Head, Usability and Risk Management at Sanofi Mannheim Area, Germany - Medical Devices for the next SES Webinar:

5/21/2014
When: 5/21/2014
1:00 PM
Contact: Mike Morrelll
309-716-6504


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Please join our speaker Molly Follette Story, PhD,
Head, Usability and Risk Management at Sanofi
Mannheim Area, Germany - Medical Devices

for the next SES Webinar:

We’re Only Human:  Addressing Human Imperfections
and Variability in Standards Work
Wednesday, May 21, 2014 from 1:00 – 2:30pm ET
Free to SES Members, $50 for non-members
The webinar will be moderated and there will be opportunity for questions.

About the Webinar:
This webinar will consider the ways in which people vary and the implications for standards development. It will discuss the variety and variability of attributes of human beings, and introduce the subject of human factors.  It will also provide an overview of the new Draft International Standard (DIS) of the ISO/IEC document: Guide 71, Guide for addressing accessibility in standards.  The purpose of the Guide is to assist standards developers in addressing accessibility in standards that focus, whether directly or indirectly, on any type of system that people use.  The Guide provides guidance for writing accessibility requirements and recommendations that would be appropriate for a specific standard.  Finally, the Guide identifies issues to consider in support of accessibility of the standards development process itself.

LEVEL:  Beginner

About the Speaker:

MOLLY FOLLETTE STORY, PhD is Head, Global Usability Engineering and Risk Assessment at Sanofi. She was formerly Human Factors and Accessible Medical Technology Specialist at the U.S. Food and Drug Administration (FDA), Center for Devices and Radiological Health (CDRH), Office of Device Evaluation (ODE), where she had an appointment to the Senior Biomedical Research Service. Previously, she served as a Senior Program Officer at the National Research Council of The National Academies. Before that she was Principal of Human Spectrum Design, LLC and Co-Director of the Rehabilitation Engineering Research Center on Accessible Medical Instrumentation.

 

Dr. Story is an expert in human factors engineering of medical devices, with particular expertise in universal design of products and in the accessibility and usability of medical instrumentation. She has served as a research and design consultant to a variety of companies and has been granted six utility patents. She was co-editor of Medical Instrumentation: Accessibility and Usability Considerations (CRC Press, 2007). She also coordinated development of and co-authored the Principles of Universal Design and co-authored The Universal Design File: Designing for People of All Ages and Abilities (North Carolina State University, 1998).

 

Dr. Story is a member of AAMI and HFES, and was previously co-chair of AAMI’s Human Factors Engineering Committee. She received a BSE from Princeton University, a MS from Stanford University, and a MS and a PhD from the School of Public Health at the University of California, Berkeley.

 

This Webinar is sponsored by Techstreet 

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11/16/2016
SES November 2016 Webinar SES-3 - The Essential Framework for Joint Standards Development


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