United States · Bill · HR
H.R. 6163 (112th)
National Pediatric Research Network Act of 2012
Introduced
19 July 2012
Last action
20 September 2012 · Introduced
Status
Received in the Senate and Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Sponsors
Cathy Rodgers, Rep. Capps, Lois [D-CA-24], Gregg Harper, Rep. DeGette, Diana [D-CO-1], PETER KING, Rep. Stearns, Cliff [R-FL-6], Rep. McCaul, Michael T. [R-TX-10], Rep. Bachus, Spencer [R-AL-6], Rep. Castor, Kathy [D-FL-14], Rep. Schwartz, Allyson Y. [D-PA-13], Rep. Matsui, Doris O. [D-CA-7]
Subjects
Healthcare
Source updated
5 December 2025
Summary
National Pediatric Research Network Act of 2012 - Amends the Public Health Service Act to authorize the Director of the National Institutes of Health (NIH), in carrying out the Pediatric Research Initiative, to act through the Director of the Eunice Kennedy Shriver National Institute of Child Health and Human Development and in collaboration with other appropriate national research institutes and national centers that carry out activities involving pediatric research to provide for the establishment of a National Pediatric Research Network. Authorizes the Director of the Institute to award cooperative agreements and grants to public or private nonprofit entities for: (1) planning, establishing, or strengthening pediatric research consortia; and (2) providing basic operating support for such consortia, including for pediatric research needs and training. Authorizes the Director to make awards for not more than 20 pediatric research consortia. Requires the Director to provide for the coordination of activities among the consortia and to require the periodic preparation and submission of reports on their activities. Requires the Director of NIH to ensure that an appropriate number of such awards are awarded to consortia that agree to: (1) focus primarily on pediatric rare diseases or conditions; (2) conduct or coordinate multi-site clinical trials of therapies for, or approaches to, the prevention, diagnosis, or treatment of pediatric rare diseases or conditions; and (3) disseminate trial findings. Requires the Director of NIH to establish a data coordinating center to: (1) distribute such findings; (2) provide assistance in the design and conduct of collaborative research projects and the management, analysis, and storage of data associated with such projects; (3) organize and conduct multi-site monitoring activities; (4) provide assistance to the Centers for Disease Control and Prevention (CDC) in the establishment of patient registries; and (5) report regularly on consortia research.
This text is taken from the official record. PoliticalRepo does not editorialize.
Timeline
19 July 2012
Introduced
Referred to the House Committee on Energy and Commerce.
Source: IntroReferral
19 July 2012
Introduced
Introduced in House
Source: IntroReferral
19 July 2012
Introduced
Introduced in House
Source: IntroReferral
20 July 2012
Referred
Referred to the Subcommittee on Health.
Source: Committee
11 September 2012
Committee
Forwarded by Subcommittee to Full Committee .
Source: Committee
11 September 2012
Committee
Subcommittee Hearings Held.
Source: Committee
19 September 2012
Passed
Motion to reconsider laid on the table Agreed to without objection.
Source: Floor
19 September 2012
Passed
On motion to suspend the rules and pass the bill, as amended Agreed to by voice vote. (text: CR H6138)
Source: Floor
19 September 2012
Passed
Passed/agreed to in House: On motion to suspend the rules and pass the bill, as amended Agreed to by voice vote.(text: CR H6138)
Source: Floor
19 September 2012
Floor
DEBATE - The House proceeded with forty minutes of debate on H.R. 6163.
Source: Floor
19 September 2012
Floor
Considered under suspension of the rules. (consideration: CR H6138-61340)
Source: Floor
19 September 2012
Floor
Mr. Upton moved to suspend the rules and pass the bill, as amended.
Source: Floor
20 September 2012
Introduced
Received in the Senate and Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
Source: IntroReferral
Votes
No vote records are attached yet.
Versions
- Referred in Senate · 20 September 2012 · Official file
- Engrossed in House · 19 September 2012 · Official file
- Introduced in House · 19 July 2012 · Official file
Documents
8 official files
Referred in Senate (text)
Referred in Senate (text)
Referred in Senate · EN · 20 September 2012
Referred in Senate (PDF)
Referred in Senate · EN · 20 September 2012
Engrossed in House (text)
Engrossed in House · EN · 19 September 2012
Engrossed in House (PDF)
Engrossed in House · EN · 19 September 2012
Passed House amended
summary · EN · 19 September 2012
Introduced in House (text)
Introduced in House · EN · 19 July 2012
Introduced in House (PDF)
Introduced in House · EN · 19 July 2012
Introduced in House
summary · EN · 19 July 2012
Sponsors
- Cathy Rodgers · R · Sponsor
- Rep. Capps, Lois [D-CA-24] · D · Sponsor
- Gregg Harper · R · Sponsor
- Rep. DeGette, Diana [D-CO-1] · D · Sponsor
- PETER KING · R · Sponsor
- Rep. Stearns, Cliff [R-FL-6] · R · Cosponsor
- Rep. McCaul, Michael T. [R-TX-10] · R · Cosponsor
- Rep. Bachus, Spencer [R-AL-6] · R · Cosponsor
- Rep. Castor, Kathy [D-FL-14] · D · Cosponsor
- Rep. Schwartz, Allyson Y. [D-PA-13] · D · Cosponsor
- Rep. Matsui, Doris O. [D-CA-7] · D · Cosponsor
- · sshr00 · Standing
- · hsif00 · Standing
Related records
- related to ← National Pediatric Research Network Act of 2012
Sources
PoliticalRepo is an index and interpretation layer, not the authoritative legal source.
- Official source: https://www.congress.gov/bill/112th-congress/house-bill/6163
- Open data entity: https://api.congress.gov/v3/bill/112/hr/6163
- us · 112-hr-6163 · source updated 5 December 2025