The Secretary, acting through the Commissioner of Food and Drugs, may enter into collaborative agreements, to be known as Critical Path Public-Private Partnerships, with one or more eligible entities to implement the Critical Path Initiative of the Food and Drug Administration by developing innovative, collaborative projects in research, education, and outreach for the purpose of fostering medical product innovation, enabling the acceleration of medical product development, manufacturing, and translational therapeutics, and enhancing medical product safety.
(b) Eligible entity
In this section, the term “eligible entity” means an entity that meets each of the following:
(1)The entity is—
(A)an institution of higher education (as such term is defined in section
1001 of title
20) or a consortium of such institutions; or
(B)an organization described in section
501(c)(3) of title
26 and exempt from tax under section 501(a) of such title.
(2)The entity has experienced personnel and clinical and other technical expertise in the biomedical sciences, which may include graduate training programs in areas relevant to priorities of the Critical Path Initiative.
(3)The entity demonstrates to the Secretary’s satisfaction that the entity is capable of—
(A)developing and critically evaluating tools, methods, and processes—
(i)to increase efficiency, predictability, and productivity of medical product development; and
(ii)to more accurately identify the benefits and risks of new and existing medical products;
(B)establishing partnerships, consortia, and collaborations with health care practitioners and other providers of health care goods or services; pharmacists; pharmacy benefit managers and purchasers; health maintenance organizations and other managed health care organizations; health care insurers; government agencies; patients and consumers; manufacturers of prescription drugs, biological products, diagnostic technologies, and devices; and academic scientists; and
(C)securing funding for the projects of a Critical Path Public-Private Partnership from Federal and nonfederal governmental sources, foundations, and private individuals.
The Secretary may not enter into a collaborative agreement under subsection (a) unless the eligible entity involved provides an assurance that the entity will not accept funding for a Critical Path Public-Private Partnership project from any organization that manufactures or distributes products regulated by the Food and Drug Administration unless the entity provides assurances in its agreement with the Food and Drug Administration that the results of the Critical Path Public-Private Partnership project will not be influenced by any source of funding.
(d) Annual report
Not later than 18 months after September 27, 2007, and annually thereafter, the Secretary, in collaboration with the parties to each Critical Path Public-Private Partnership, shall submit a report to the Committee on Health, Education, Labor, and Pensions of the Senate and the Committee on Energy and Commerce of the House of Representatives—
(1)reviewing the operations and activities of the Partnerships in the previous year; and
(2)addressing such other issues relating to this section as the Secretary determines to be appropriate.
In this section, the term “medical product” includes a drug, a biological product as defined in section
262 of title
42, a device, and any combination of such products.
(f) Authorization of appropriations
To carry out this section, there is authorized to be appropriated $6,000,000 for each of fiscal years 2013 through 2017.
The table below lists the classification updates, since Jan. 3, 2012, for this section. Updates to a broader range of sections may be found at the update page for containing chapter, title, etc.
The most recent Classification Table update that we have noticed was Tuesday, August 13, 2013
An empty table indicates that we see no relevant changes listed in the classification tables. If you suspect that our system may be missing something, please double-check with the Office of the Law Revision Counsel.