Welcome to the web pages for the Rehabilitation Engineering Research Center on Accessible Medical Instrumentation (RERC-AMI)

Our aim is to address the critical need for new medical instrumentation technologies that are universally accessible to all people

 

[ Overview ] [ Partners and Advisors ]
[ Research and Development Projects ] [ Information and Events ]
[ Tech Reports and Product Tables ] [ Training ]
[ Publications ] [ Links ]

 

Federal funding for this Center, from the National Institute on Disability and Rehabilitation Research (NIDRR), U.S. Department of Education, ended in July 2008. Most of the content on the above web pages has not been updated since 2007 or 2008, but will continue to be available through at least 2011.

Direct link to some key pages (added 2010):

 


Extracted from the Patient Protection and Affordable Care Act of 2010 (with some text bolded for effect):

"... SEC. 4203. REMOVING BARRIERS AND IMPROVING ACCESS TO WELLNESS FOR INDIVIDUALS WITH DISABILITIES. Title V of the Rehabilitation Act of 1973 (29 U.S.C. 791 et seq.) is amended by adding at the end of the following:

SEC. 510. ESTABLISHMENT OF STANDARDS FOR ACCESSIBLE MEDICAL DIAGNOSTIC EQUIPMENT.

(a) Standards - Not later than 24 months after the date of enactment of the Affordable Health Choices Act, the Architectural and Transportation Barriers Compliance Board shall, in consultation with the Commissioner of the Food and Drug Administration, promulgate regulatory standards in accordance with the Administrative Procedure Act setting forth the minimum technical criteria for medical diagnostic equipment used in (or in conjunction with) physician's offices, clinics, emergency rooms, hospitals, and other medical settings. The standards shall ensure that such equipment is accessible to, and usable by, individuals with accessibility needs, and shall allow independent entry to, use of, and exit from the equipment by such individuals to the maximum extent possible.

(b) Medical Diagnostic Equipment Covered - The standards issued under subsection (a) for medical diagnostic equipment shall apply to equipment that includes examination tables, examination chairs (including chairs used for eye examinations or procedures, and dental examinations or procedures), weight scales, mammography equipment, x-ray machines, and other radiological equipment commonly used for diagnostic purposes by health professionals.

(c) Review and Amendment - The Architectural and Transportation Barriers Compliance Board, in consultation with the Commissioner of the Food and Drug Administration, shall periodically review and, as appropriate, amend the standards in accordance with the Administrative Procedure Act. ..."

 

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