H.R.2695 - Trisomy 21 Research Centers of Excellence Act of 2011112th Congress (2011-2012)
|Sponsor:||Rep. McMorris Rodgers, Cathy [R-WA-5] (Introduced 07/29/2011)|
|Committees:||House - Energy and Commerce|
|Latest Action:||08/05/2011 Referred to the Subcommittee on Health. (All Actions)|
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Summary: H.R.2695 — 112th Congress (2011-2012)All Bill Information (Except Text)
Introduced in House (07/29/2011)
Trisomy 21 Research Centers of Excellence of 2011- Amends the Public Health Service Act to require the Director of the National Institutes of Health (NIH), acting through the Director of the Eunice Kennedy Shriver National Institute of Child Health and Human Development, to expand and intensify NIH programs with respect to research and related activities concerning Down syndrome. Requires the Director of NIH to publish a research plan on Down syndrome and update it every five years or as appropriate.
Requires the Director of NIH to award grants and contracts to public or nonprofit private entities to pay all or part of the cost of planning, establishing, improving, and providing basic operating support for centers of excellence regarding translational research on Down syndrome. Sets forth requirements for such centers, which shall include: (1) contributing to a comprehensive research portfolio for Down syndrome, (2) having a primary focus on Down syndrome, (3) providing an optimal venue and infrastructure for patient-oriented research, and (4) conducting basic, clinical, and translational research on Down syndrome in specified areas.
Authorizes the Director of NIH to establish a Down Syndrome Consortium to facilitate the exchange of information and to make the research effort on Down syndrome more efficient and effective.