42 USC 299b-7 - Research on outcomes of health care items and services

U.S Code last checked for updates: Aug 01, 2025

§ 299b–7.

Research on outcomes of health care items and services

(a)

Research, demonstrations, and evaluations

(1)

Improvement of effectiveness and efficiency

(A)

In general

To improve the quality, effectiveness, and efficiency of health care delivered pursuant to the programs established under titles XVIII, XIX, and XXI of the Social Security Act [42 U.S.C. 1395 et seq., 1396 et seq., 1397aa et seq.], the Secretary 1

 So in original. Probably should be followed by a comma.

acting through the Director of the Agency for Healthcare Research and Quality (in this section referred to as the “Director”), shall conduct and support research to meet the priorities and requests for scientific evidence and information identified by such programs with respect to—

(i)

the outcomes, comparative clinical effectiveness, and appropriateness of health care items and services (including prescription drugs); and

(ii)

strategies for improving the efficiency and effectiveness of such programs, including the ways in which such items and services are organized, managed, and delivered under such programs.

(B)

Specification

(2)

Priorities

(A)

In general

(B)

Initial list

(C)

Process

In carrying out subparagraph (A), the Secretary—

(i)

shall ensure that there is broad and ongoing consultation with relevant stakeholders in identifying the highest priorities for research, demonstrations, and evaluations to support and improve the programs established under titles XVIII, XIX, and XXI of the Social Security Act [42 U.S.C. 1395 et seq., 1396 et seq., 1397aa et seq.];

(ii)

may include health care items and services which impose a high cost on such programs, as well as those which may be underutilized or overutilized and which may significantly improve the prevention, treatment, or cure of diseases and conditions (including chronic conditions) which impose high direct or indirect costs on patients or society; and

(iii)

shall ensure that the research and activities undertaken pursuant to this section are responsive to the specified priorities and are conducted in a timely manner.

(3)

Evaluation and synthesis of scientific evidence

(A)

In general

The Secretary shall—

(i)

evaluate and synthesize available scientific evidence related to health care items and services (including prescription drugs) identified as priorities in accordance with paragraph (2) with respect to the comparative clinical effectiveness, outcomes, appropriateness, and provision of such items and services (including prescription drugs);

(ii)

identify issues for which existing scientific evidence is insufficient with respect to such health care items and services (including prescription drugs);

(iii)

disseminate to prescription drug plans and MA–PD plans under part D of title XVIII of the Social Security Act [42 U.S.C. 1395w–101 et seq.], other health plans, and the public the findings made under clauses (i) and (ii); and

(iv)

work in voluntary collaboration with public and private sector entities to facilitate the development of new scientific knowledge regarding health care items and services (including prescription drugs).

(B)

Initial research

(C)

Dissemination

(i)

In general

To enhance patient safety and the quality of health care, the Secretary shall make available and disseminate in appropriate formats to prescription drugs plans under part D, and MA–PD plans under part C, of title XVIII of the Social Security Act [42 U.S.C. 1395w–101 et seq., 1395w–21 et seq.], other health plans, and the public the evaluations and syntheses prepared pursuant to subparagraph (A) and the findings of research conducted pursuant to paragraph (1). In carrying out this clause the Secretary, in order to facilitate the availability of such evaluations and syntheses or findings at every decision point in the health care system, shall—

(I)

present such evaluations and syntheses or findings in a form that is easily understood by the individuals receiving health care items and services (including prescription drugs) under such plans and periodically assess that the requirements of this subclause have been met; and

(II)

provide such evaluations and syntheses or findings and other relevant information through easily accessible and searchable electronic mechanisms, and in hard copy formats as appropriate.

(ii)

Rule of construction

Nothing in this section shall be construed as—

(I)

affecting the authority of the Secretary or the Commissioner of Food and Drugs under the Federal Food, Drug, and Cosmetic Act [21 U.S.C. 301 et seq.] or the Public Health Service Act [42 U.S.C. 201 et seq.]; or

(II)

conferring any authority referred to in subclause (I) to the Director.

(D)

Accountability

In carrying out this paragraph, the Secretary shall implement activities in a manner that—

(i)

makes publicly available all scientific evidence relied upon and the methodologies employed, provided such evidence and method are not protected from public disclosure by section 1905 of title 18 or other applicable law so that the results of the research, analyses, or syntheses can be evaluated or replicated; and

(ii)

ensures that any information needs and unresolved issues identified in subparagraph (A)(ii) are taken into account in priority-setting for future research conducted by the Secretary.

(4)

Confidentiality

(A)

In general

(B)

Rule of construction

(5)

Evaluations

(6)

Improving information available to health care providers, patients, and policymakers

Not later than 18 months after December 8, 2003, the Secretary shall identify options that could be undertaken in voluntary collaboration with private and public entities (as appropriate) for the—

(A)

provision of more timely information through the programs established under titles XVIII, XIX, and XXI of the Social Security Act [42 U.S.C. 1395

et seq., 1396 et seq., 1397aa et seq.], regarding the outcomes and quality of patient care, including clinical and patient-reported outcomes, especially with respect to interventions and conditions for which clinical trials would not be feasible or raise ethical concerns that are difficult to address;

(B)

acceleration of the adoption of innovation and quality improvement under such programs; and

(C)

development of management tools for the programs established under titles XIX and XXI of the Social Security Act [42 U.S.C. 1396 et seq., 1397aa et seq.], and with respect to the programs established under such titles, assess the feasibility of using administrative or claims data, to—

(i)

improve oversight by State officials;

(ii)

support Federal and State initiatives to improve the quality, safety, and efficiency of services provided under such programs; and

(iii)

provide a basis for estimating the fiscal and coverage impact of Federal or State program and policy changes.

(b)

Recommendations

(1)

Disclaimer

In carrying out this section, the Director shall—

(A)

not mandate national standards of clinical practice or quality health care standards; and

(B)

include in any recommendations resulting from projects funded and published by the Director, a corresponding reference to the prohibition described in subparagraph (A).

(2)

Requirement for implementation

(3)

Rule of construction

(c)

Research with respect to dissemination

(d)

Limitation on CMS

(e)

Authorization of appropriations

(Pub. L. 108–173, title X, § 1013, Dec. 8, 2003, 117 Stat. 2438.)

cite as: 42 USC 299b-7