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42 U.S.C. § 300aa–2Program responsibilities

submitted 82 years ago by Pub. L. 99-660 to r/title-42-THE-PUBLIC-HEALTH-AND-WELFARE · 704 words · no verdicts yet

in plain englishAI-generated · not legal advice

The Director of the Program must guide federal work on vaccines. This covers research, development, safety testing, licensing, production, distribution, and evaluating side effects. The Director does this through a plan and must consult every agency involved.

(a) This section lists nine jobs the Director of the Program must do. The Director does each job through the plan required by section 300aa–3. (1) Vaccine research: The Director must guide and coordinate research at the National Institutes of Health, the Centers for Disease Control and Prevention, the FDA's Office of Biologics Research and Review, the Department of Defense, and the Agency for International Development. This research is about building human immunity to diseases and preventing bad reactions to vaccines. (2) Vaccine development: The Director must guide work at NIH, the FDA's biologics office, the Department of Defense, and the Agency for International Development to build the techniques needed to make safe, effective vaccines. (3) Safety and efficacy testing: The Director must guide vaccine safety and effectiveness testing done at NIH, the CDC, the FDA's biologics office, the Department of Defense, and the Agency for International Development. (4) Licensing: The Director must guide how resources are used to run the vaccine-licensing program under section 263a. (5) Production and procurement: The Director must make sure that government and private production of safe, effective vaccines meets the needs of the U.S. population. It must also meet U.S. promises to prevent infectious disease in other countries. (6) Distribution and use: The Director must guide the CDC and help states, local governments, and health providers distribute and use vaccines. This includes work to get the public to accept immunizations and to make providers and the public aware of possible side effects and reasons not to give a vaccine. (7) Evaluating vaccines and immunization activities: The Director must guide NIH, the CDC, the FDA's biologics office, the National Center for Health Statistics, the National Center for Health Services Research and Health Care Technology Assessment, and the Centers for Medicare & Medicaid Services. Together they must watch how much vaccines and immunization programs are needed, how well they work, and what side effects they cause. (8) Coordinating government and non-government work: The Director must help federal agencies share information with private companies and groups that develop and produce vaccines or do vaccine research. The Director must also encourage private groups to put their own money into work that supports the government's efforts. (9) Funding federal agencies: The Director must give federal agencies working on the plan extra money, from funds appropriated under section 300aa–6, on top of what they already have for this work. (b) While doing the work in subsection (a) and writing the plan under section 300aa–3, the Director must talk with every federal agency involved in vaccine research, development, testing, licensing, production, buying, distributing, and use.
the actual law source: uscode.house.gov ↗public domain
(a)

The Director of the Program shall have the following responsibilities:

(1) Vaccine research

The Director of the Program shall, through the plan issued under section 300aa–3 of this title, coordinate and provide direction for research carried out in or through the National Institutes of Health, the Centers for Disease Control and Prevention, the Office of Biologics Research and Review of the Food and Drug Administration, the Department of Defense, and the Agency for International Development on means to induce human immunity against naturally occurring infectious diseases and to prevent adverse reactions to vaccines.

(2) Vaccine development

The Director of the Program shall, through the plan issued under section 300aa–3 of this title, coordinate and provide direction for activities carried out in or through the National Institutes of Health, the Office of Biologics Research and Review of the Food and Drug Administration, the Department of Defense, and the Agency for International Development to develop the techniques needed to produce safe and effective vaccines.

(3) Safety and efficacy testing of vaccines

The Director of the Program shall, through the plan issued under section 300aa–3 of this title, coordinate and provide direction for safety and efficacy testing of vaccines carried out in or through the National Institutes of Health, the Centers for Disease Control and Prevention, the Office of Biologics Research and Review of the Food and Drug Administration, the Department of Defense, and the Agency for International Development.

(4) Licensing of vaccine manufacturers and vaccines

The Director of the Program shall, through the plan issued under section 300aa–3 of this title, coordinate and provide direction for the allocation of resources in the implementation of the licensing program under section 263a of this title.

(5) Production and procurement of vaccines

The Director of the Program shall, through the plan issued under section 300aa–3 of this title, ensure that the governmental and non-governmental production and procurement of safe and effective vaccines by the Public Health Service, the Department of Defense, and the Agency for International Development meet the needs of the United States population and fulfill commitments of the United States to prevent human infectious diseases in other countries.

(6) Distribution and use of vaccines

The Director of the Program shall, through the plan issued under section 300aa–3 of this title, coordinate and provide direction to the Centers for Disease Control and Prevention and assistance to States, localities, and health practitioners in the distribution and use of vaccines, including efforts to encourage public acceptance of immunizations and to make health practitioners and the public aware of potential adverse reactions and contraindications to vaccines.

(7) Evaluating the need for and the effectiveness and adverse effects of vaccines and immunization activities

The Director of the Program shall, through the plan issued under section 300aa–3 of this title, coordinate and provide direction to the National Institutes of Health, the Centers for Disease Control and Prevention, the Office of Biologics Research and Review of the Food and Drug Administration, the National Center for Health Statistics, the National Center for Health Services Research and Health Care Technology Assessment, and the Centers for Medicare & Medicaid Services in monitoring the need for and the effectiveness and adverse effects of vaccines and immunization activities.

(8) Coordinating governmental and non-governmental activities

The Director of the Program shall, through the plan issued under section 300aa–3 of this title, provide for the exchange of information between Federal agencies involved in the implementation of the Program and non-governmental entities engaged in the development and production of vaccines and in vaccine research and encourage the investment of non-governmental resources complementary to the governmental activities under the Program.

(9) Funding of Federal agencies

The Director of the Program shall make available to Federal agencies involved in the implementation of the plan issued under section 300aa–3 of this title funds appropriated under section 300aa–6 of this title to supplement the funds otherwise available to such agencies for activities under the plan.

(b)

In carrying out subsection (a) and in preparing the plan under section 300aa–3 of this title, the Director shall consult with all Federal agencies involved in research on and development, testing, licensing, production, procurement, distribution, and use of vaccines.

Source credit: (July 1, 1944, ch. 373, title XXI, § 2102, as added Pub. L. 99–660, title III, § 311(a), Nov. 14, 1986, 100 Stat. 3756; amended Pub. L. 102–531, title III, § 312(d)(13), Oct. 27, 1992, 106 Stat. 3505; Pub. L. 108–173, title IX, § 900(e)(2)(F), Dec. 8, 2003, 117 Stat. 2372.)

history & why it existsrecord from the source credit
  • 1944Enacted · Pub. L. 99-660 · 100 Stat. 3756
  • 1992Amended · Pub. L. 102-531 · 106 Stat. 3505
  • 2003Amended · Pub. L. 108-173 · 117 Stat. 2372

A history note hasn’t been published yet. The record shows enactment by Pub. L. 99-660 on 1944-07-01.

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