Federal
COVID–19 Emergency Medical Supplies Enhancement Act of 2020
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I
116TH CONGRESS
2D SESSION
H. R. 6858
To enhance authorities under the Defense Production Act of 1950 to respond
to the COVID–19 emergency, to provide additional oversight of such
authorities, and to require a strategy on securing supply chains for
medical materials, and for other purposes.
IN THE HOUSE OF REPRESENTATIVES
MAY 13, 2020
Mr. VARGAS (for himself, Ms. WATERS, Mr. CROW, Mr. RYAN, Mrs. TRAHAN,
and Ms. SLOTKIN) introduced the following bill; which was referred to the
Committee on Financial Services, and in addition to the Committee on
Energy and Commerce, for a period to be subsequently determined by the
Speaker, in each case for consideration of such provisions as fall within
the jurisdiction of the committee concerned
A BILL
To enhance authorities under the Defense Production Act
of 1950 to respond to the COVID–19 emergency, to
provide additional oversight of such authorities, and to
require a strategy on securing supply chains for medical
materials, and for other purposes.
Be it enacted by the Senate and House of Representa-
1
tives of the United States of America in Congress assembled,
2
SECTION 1. SHORT TITLE.
3
This Act may be cited as the ‘‘COVID–19 Emergency
4
Medical Supplies Enhancement Act of 2020’’.
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SEC. 2. DETERMINATION ON EMERGENCY SUPPLIES AND
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RELATIONSHIP TO STATE AND LOCAL EF-
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FORTS.
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(a) DETERMINATION.—For the purposes of section
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101 of the Defense Production Act of 1950 (50 U.S.C.
5
4511), the following materials shall be deemed to be scarce
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and critical materials essential to the national defense and
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otherwise meet the requirements of section 101(b) of such
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Act during the COVID–19 emergency period:
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(1) Diagnostic tests, including serological tests,
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for COVID–19 and the reagents and other materials
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necessary for producing or conducting such tests.
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(2) Personal protective equipment, including
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face shields, N–95 respirator masks, and any other
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masks determined by the Secretary of Health and
15
Human Services to be needed to respond to the
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COVID–19 pandemic, and the materials to produce
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such equipment.
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(3) Medical ventilators, the components nec-
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essary to make such ventilators, and medicines need-
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ed to use a ventilator as a treatment for any indi-
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vidual who is hospitalized for COVID–19.
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(4) Pharmaceuticals and any medicines deter-
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mined by the Food and Drug Administration or an-
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other Government agency to be effective in treating
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COVID–19 (including vaccines for COVID–19) and
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•HR 6858 IH
any materials necessary to produce or use such
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pharmaceuticals or medicines (including self-injec-
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tion syringes or other delivery systems).
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(5) Any other medical equipment or supplies
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determined by the Secretary of Health and Human
5
Services or the Secretary of Homeland Security to
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be scarce and critical materials essential to the na-
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tional defense for purposes of section 101 of the De-
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fense Production Act of 1950 (50 U.S.C. 4511).
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(b) EXERCISE OF TITLE I AUTHORITIES IN RELA-
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TION TO CONTRACTS BY STATE AND LOCAL GOVERN-
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MENTS.—In exercising authorities under title I of the De-
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fense Production Act of 1950 (50 U.S.C. 4511 et seq.)
13
during the COVID–19 emergency period, the President
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(and any officer or employee of the United States to which
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authorities under such title I have been delegated)—
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(1) may exercise the prioritization or allocation
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authority provided in such title I to exclude any ma-
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terials described in subsection (a) ordered by a State
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or local government that are scheduled to be deliv-
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ered within 15 days of the time at which—
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(A) the purchase order or contract by the
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Federal Government for such materials is
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made; or
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(B) the materials are otherwise allocated
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by the Federal Government under the authori-
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ties contained in such Act; and
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(2) shall, within 24 hours of any exercise of the
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prioritization or allocation authority provided in such
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title I—
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(A) notify any State or local government if
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the exercise of such authorities would delay the
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receipt of such materials ordered by such gov-
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ernment; and
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(B) take such steps as may be necessary to
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ensure that such materials ordered by such gov-
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ernment are delivered in the shortest possible
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period.
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(c) UPDATE TO THE FEDERAL ACQUISITION REGU-
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LATION.—Not later than 15 days after the date of the en-
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actment of this Act, the Federal Acquisition Regulation
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shall be revised to reflect the requirements of subsection
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(b)(1).
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SEC. 3. ENGAGEMENT WITH THE PRIVATE SECTOR.
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(a) SENSE OF CONGRESS.—The Congress—
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(1) appreciates the willingness of private com-
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panies not traditionally involved in producing items
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for the health sector to volunteer to use their exper-
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tise and supply chains to produce essential medical
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supplies and equipment;
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(2) encourages other manufacturers to review
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their existing capacity and to develop capacity to
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produce essential medical supplies, medical equip-
5
ment, and medical treatments to address the
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COVID–19 emergency; and
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(3) commends and expresses deep appreciation
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to individual citizens who have been producing per-
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sonal protective equipment and other materials for,
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in particular, use at hospitals in their community.
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(b) OUTREACH REPRESENTATIVE.—
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(1) DESIGNATION.—Consistent with the au-
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thorities in title VII of the Defense Production Act
14
of 1950 (50 U.S.C. 4551 et seq.), the Administrator
15
of the Federal Emergency Management Agency, in
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consultation with the Secretary of Health and
17
Human Services, shall designate or shall appoint,
18
pursuant to section 703 of such Act (50 U.S.C.
19
4553), an individual to be known as the ‘‘Outreach
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Representative’’. Such individual shall—
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(A) be appointed from among individuals
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with substantial experience in the private sector
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in the production of medical supplies or equip-
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ment; and
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(B) act as the Government-wide single
1
point of contact during the COVID–19 emer-
2
gency for outreach to manufacturing companies
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and their suppliers who may be interested in
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producing medical supplies or equipment, in-
5
cluding the materials described under section 2.
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(2) ENCOURAGING PARTNERSHIPS.—The Out-
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reach Representative shall seek to develop partner-
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ships between companies, in coordination with the
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Supply Chain Stabilization Task Force or any over-
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all coordinator appointed by the President to oversee
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the response to the COVID–19 emergency, including
12
through the exercise of the authorities under section
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708 of the Defense Production Act of 1950 (50
14
U.S.C. 4558).
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SEC. 4. ENHANCEMENT OF SUPPLY CHAIN PRODUCTION.
16
In exercising authority under title III of the Defense
17
Production Act of 1950 (50 U.S.C. 4531 et seq.) with re-
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spect to materials described in section 2, the President
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shall seek to ensure that support is provided to companies
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that comprise the supply chains for reagents, components,
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raw materials, and other materials and items necessary
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to produce or use the materials described in section 2.
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SEC. 5. OVERSIGHT OF CURRENT ACTIVITY AND NEEDS.
24
(a) RESPONSE TO IMMEDIATE NEEDS.—
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(1) IN GENERAL.—Not later than 7 days after
1
the date of the enactment of this Act, the President,
2
in coordination with the National Response Coordi-
3
nation Center of the Federal Emergency Manage-
4
ment Agency, the Administrator of the Defense Lo-
5
gistics Agency, the Secretary of Health and Human
6
Services, the Secretary of Veterans Affairs, and
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heads of other Federal agencies (as appropriate),
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shall submit to the appropriate congressional com-
9
mittees a report assessing the immediate needs de-
10
scribed in paragraph (2) to combat the COVID–19
11
pandemic and the plan for meeting those immediate
12
needs.
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(2) ASSESSMENT.—The report required by this
14
subsection shall include—
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(A) an assessment of the needs for medical
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supplies or equipment necessary to address the
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needs of the population of the United States in-
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fected by the virus SARS–CoV–2 that causes
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COVID–19 and to prevent an increase in the
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incidence of COVID–19 throughout the United
21
States, including diagnostic tests, serological
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tests, medicines that have been approved by the
23
Food and Drug Administration to treat
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COVID–19, and ventilators and medicines
1
needed to employ ventilators;
2
(B) based on meaningful consultations
3
with relevant stakeholders, an assessment of the
4
need for personal protective equipment and
5
other supplies (including diagnostic tests) re-
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quired by—
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(i) health professionals, health work-
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ers, and hospital staff;
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(ii) workers in industries and sectors
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described in the ‘‘Advisory Memorandum
11
on Identification of Essential Critical In-
12
frastructure Workers during the COVID–
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19 Response’’ issued by the Director of
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Cybersecurity and Infrastructure Security
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Agency of the Department of Homeland
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Security on April 17, 2020 (and any ex-
17
pansion of industries and sectors included
18
in updates to such advisory memorandum);
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and
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(iii) other workers determined to be
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essential based on such consultation;
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(C) an assessment of the quantities of
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equipment and supplies in the Strategic Na-
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tional Stockpile (established under section
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319F–2 of the Public Health Service Act (42
1
U.S.C. 247d–6b(a)(1))) as of the date of the re-
2
port, and the projected gap between the quan-
3
tities of equipment and supplies identified as
4
needed in the assessment under subparagraphs
5
(A) and (B) and the quantities in the Strategic
6
National Stockpile;
7
(D) an identification of the industry sec-
8
tors and manufacturers most ready to fulfill
9
purchase orders for such equipment and sup-
10
plies (including manufacturers that may be
11
incentivized) through the exercise of authority
12
under section 303(e) of the Defense Production
13
Act of 1950 (50 U.S.C. 4533(e)) to modify, ex-
14
pand, or improve production processes to manu-
15
facture such equipment and supplies to respond
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immediately to a need identified in subpara-
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graph (A) or (B);
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(E) an identification of Government-owned
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and privately-owned stockpiles of such equip-
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ment and supplies not included in the Strategic
21
National Stockpile that could be repaired or re-
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furbished;
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(F) an identification of previously distrib-
1
uted critical supplies that can be redistributed
2
based on current need;
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(G) a description of any exercise of the au-
4
thorities described under subsection (a)(5) or
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(b)(1) of section 2; and
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(H) an identification of critical areas of
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need, by county and by areas identified by the
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Indian Health Service, in the United States and
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the metrics and criteria for identification as a
10
critical area.
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(3) PLAN.—The report required by this sub-
12
section shall include a plan for meeting the imme-
13
diate needs to combat the COVID–19 pandemic, in-
14
cluding the needs described in paragraph (1). Such
15
plan shall include—
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(A) each contract the Federal Government
17
has entered into to meet such needs, including
18
the purpose of each contract, the type and
19
amount of equipment, supplies, or services to be
20
provided under the contract, the entity per-
21
forming such contract, and the dollar amount
22
of each contract;
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(B) each contract that the Federal Govern-
24
ment intends to enter into within 14 days after
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submission of such report, including the infor-
1
mation described in subparagraph (A) for each
2
such contract; and
3
(C) whether any of the contracts described
4
in subparagraph (A) or (B) have or will have a
5
priority rating under the Defense Production
6
Act of 1950 (50 U.S.C. 4501 et seq.), including
7
purchase orders pursuant to Department of De-
8
fense Directive 4400.1 (or any successor direc-
9
tive), subpart A of part 101 of title 45, Code
10
of Federal Regulations, or any other applicable
11
authority.
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(4) ADDITIONAL REQUIREMENTS.—The report
13
required by this subsection, and each update re-
14
quired by paragraph (5), shall include—
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(A) any requests for equipment and sup-
16
plies from State or local governments and In-
17
dian Tribes, and an accompanying list of the
18
employers and unions consulted in developing
19
these requests;
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(B) any modeling or formulas used to de-
21
termine allocation of equipment and supplies,
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and any related chain of command issues on
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making final decisions on allocations;
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(C) the amount and destination of equip-
1
ment and supplies delivered;
2
(D) an explanation of why any portion of
3
any contract, whether to replenish the Strategic
4
National Stockpile or otherwise, will not be
5
filled;
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(E) of products procured under this sec-
7
tion, the percentage of such products that are
8
used to replenish the Strategic National Stock-
9
pile, that are targeted to COVID–19 hotspots,
10
and that are use
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