To require the Secretary of Health and Human Services to provide for recommendations for the development and use of clinical data registries for the improvement of patient care.

3/14/2024, 12:48 PM

Congressional Summary of HR 5214

(Sec. 1) Requires the Department of Health and Human Services (HHS) to consult with clinical experts and make recommendations for the use of clinical data registries to improve patient care.

Directs HHS to include in the recommendations: (1) standards to allow exchange of information between electronic health records and registries, (2) how registries can be used to evaluate models and methods of care, (3) how registries can be used to monitor the safety and efficacy of products approved by the Food and Drug Administration (FDA), (4) how registry data can inform health care professionals on the prevention of disease and how educational resources derived from registry data can be disseminated, and (5) how registries can promote preventive health care.

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Current Status of Bill HR 5214

Bill HR 5214 is currently in the status of Bill Introduced since July 28, 2014. Bill HR 5214 was introduced during Congress 113 and was introduced to the House on July 28, 2014. Bill HR 5214's most recent activity was Placed on the Union Calendar, Calendar No. 514. as of December 22, 2014

Bipartisan Support of Bill HR 5214

Total Number of Sponsors

Democrat Sponsors

Republican Sponsors

Unaffiliated Sponsors

Total Number of Cosponsors

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Republican Cosponsors

Unaffiliated Cosponsors

Policy Area and Potential Impact of Bill HR 5214

Primary Policy Focus

Health

Potential Impact Areas

- Administrative law and regulatory procedures

- Computers and information technology

- Department of Health and Human Services

- Drug safety, medical device, and laboratory regulation

- Government information and archives

- Health care quality

- Health information and medical records

- Health promotion and preventive care

- Medical research

- Medicare

Alternate Title(s) of Bill HR 5214

To require the Secretary of Health and Human Services to provide for recommendations for the development and use of clinical data registries for the improvement of patient care.