[Congressional Record Volume 167, Number 86 (Tuesday, May 18, 2021)]
[House]
[Pages H2454-H2456]
From the Congressional Record Online through the Government Publishing Office [www.gpo.gov]




                              {time}  1300
        SECURING AMERICA'S VACCINES FOR EMERGENCIES ACT OF 2021

  Mr. CLEAVER. Mr. Speaker, I move to suspend the rules and pass the 
bill (H.R. 3146) to amend the Defense Production Act of 1950 to ensure 
the supply of certain medical materials essential to national defense, 
and for other purposes.
  The Clerk read the title of the bill.
  The text of the bill is as follows:

                               H.R. 3146

       Be it enacted by the Senate and House of Representatives of 
     the United States of America in Congress assembled,

     SECTION 1. SHORT TITLE.

       This Act may be cited as the ``Securing America's Vaccines 
     for Emergencies Act of 2021'' or the ``SAVE Act of 2021''.

     SEC. 2. SECURING ESSENTIAL MEDICAL MATERIALS.

       (a) Statement of Policy.--Section 2(b) of the Defense 
     Production Act of 1950 (50 U.S.C. 4502) is amended--
       (1) by redesignating paragraphs (3) through (8) as 
     paragraphs (4) through (9), respectively; and
       (2) by inserting after paragraph (2) the following:
       ``(3) authorities under this Act should be used when 
     appropriate to ensure the availability of medical materials 
     essential to national defense, including through measures 
     designed to secure the drug supply chain, and taking into 
     consideration the importance of United States 
     competitiveness, scientific leadership and cooperation, and 
     innovative capacity;''.
       (b) Strengthening Domestic Capability.--Section 107 of the 
     Defense Production Act of 1950 (50 U.S.C. 4517) is amended--
       (1) in subsection (a), by inserting ``(including medical 
     materials)'' after ``materials''; and
       (2) in subsection (b)(1), by inserting ``(including medical 
     materials such as drugs, devices, and biological products to 
     diagnose, cure, mitigate, treat, or prevent disease that are 
     essential to national defense)'' after ``essential 
     materials''.
       (c) Strategy on Securing Supply Chains for Medical 
     Materials.--Title I of the Defense Production Act of 1950 (50 
     U.S.C. 4511 et seq.) is amended by adding at the end the 
     following:

     ``SEC. 109. STRATEGY ON SECURING SUPPLY CHAINS FOR MEDICAL 
                   MATERIALS.

       ``(a) In General.--Not later than 180 days after the date 
     of the enactment of this section, the President, in 
     consultation with the Secretary of Health and Human Services, 
     the Secretary of Commerce, the Secretary of Homeland 
     Security, and the Secretary of Defense, shall transmit a 
     strategy to the appropriate Members of Congress that includes 
     the following:
       ``(1) A detailed plan to use the authorities under this 
     title and title III, or any other provision of law, to ensure 
     the supply of medical materials (including drugs, devices, 
     and biological products (as that term is defined in section 
     351 of the Public Health Service Act (42 U.S.C. 262)) to 
     diagnose, cure, mitigate, treat, or prevent disease) 
     essential to national defense, to the extent necessary for 
     the purposes of this Act.
       ``(2) An analysis of vulnerabilities to existing supply 
     chains for such medical materials, and recommendations to 
     address the vulnerabilities.
       ``(3) Measures to be undertaken by the President to 
     diversify such supply chains, as appropriate and as required 
     for national defense.
       ``(4) A discussion of--
       ``(A) any significant effects resulting from the plan and 
     measures described in this subsection on the production, 
     cost, or distribution of biological products (as that term is 
     defined in section 351 of the Public Health Service Act (42 
     U.S.C. 262)) or any other devices or drugs (as defined under 
     the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 301 et. 
     seq.));
       ``(B) a timeline to ensure that essential components of the 
     supply chain for medical materials are not under the 
     exclusive control of a foreign government in a manner that 
     the President determines could threaten the national defense 
     of the United States; and
       ``(C) efforts to mitigate any risks resulting from the plan 
     and measures described in this subsection to United States 
     competitiveness, scientific leadership, and innovative 
     capacity, including efforts to cooperate and proactively 
     engage with United States allies.
       ``(b) Progress Report.--Following submission of the 
     strategy under subsection (a), the President shall submit to 
     the appropriate Members of Congress an annual progress report 
     until September 30, 2025, evaluating the implementation of 
     the strategy, and may include updates to the strategy as 
     appropriate. The strategy and progress reports shall be 
     submitted in unclassified form but may contain a classified 
     annex.
       ``(c) Appropriate Members of Congress.--The term 
     `appropriate Members of Congress' means the Speaker, majority 
     leader, and minority leader of the House of Representatives, 
     the majority leader and minority leader of the Senate, the 
     Chairman and Ranking Member of the Committee on Financial 
     Services of the House of Representatives, and the Chairman 
     and Ranking Member of the Committee on Banking, Housing, and 
     Urban Affairs of the Senate.''.

     SEC. 3. INVESTMENT IN SUPPLY CHAIN SECURITY.

       (a) In General.--Section 303 of the Defense Production Act 
     of 1950 (50 U.S.C. 4533) is amended by adding at the end the 
     following:
       ``(h) Investment in Supply Chain Security.--
       ``(1) In general.--In addition to other authorities in this 
     title, the President may make available to an eligible entity 
     described in paragraph (2) payments to increase the security 
     of supply chains and supply chain activities, if the 
     President certifies to Congress not less than 30 days before 
     making such a payment that the payment is critical to meet 
     national defense requirements of the United States.
       ``(2) Eligible entity.--An eligible entity described in 
     this paragraph is an entity that--
       ``(A) is organized under the laws of the United States or 
     any jurisdiction within the United States; and
       ``(B) produces--
       ``(i) one or more critical components;
       ``(ii) critical technology; or
       ``(iii) one or more products or raw materials for the 
     security of supply chains or supply chain activities.
       ``(3) Definitions.--In this subsection, the terms `supply 
     chain' and `supply chain activities' have the meanings given 
     those terms by the President by regulation.''.
       (b) Regulations.--
       (1) In general.--Not later than 90 days after the date of 
     the enactment of this Act, the President shall prescribe 
     regulations setting forth definitions for the terms ``supply 
     chain'' and ``supply chain activities'' for the purposes of 
     section 303(h) of the Defense Production Act of 1950 (50 
     U.S.C. 4533(h)), as added by subsection (a).
       (2) Scope of definitions.--The definitions required by 
     paragraph (1)--
       (A) shall encompass--

[[Page H2455]]

       (i) the organization, people, activities, information, and 
     resources involved in the delivery and operation of a product 
     or service used by the Government; or
       (ii) critical infrastructure as defined in Presidential 
     Policy Directive 21 (February 12, 2013; relating to critical 
     infrastructure security and resilience); and
       (B) may include variations as determined necessary and 
     appropriate by the President for purposes of national 
     defense.

  The SPEAKER pro tempore. Pursuant to the rule, the gentleman from 
Missouri (Mr. Cleaver) and the gentleman from Arkansas (Mr. Hill) each 
will control 20 minutes.
  The Chair recognizes the gentleman from Missouri.


                             General Leave

  Mr. CLEAVER. Mr. Speaker, I ask unanimous consent that all Members 
may have 5 legislative days within which to revise and extend their 
remarks on this legislation and to insert extraneous material thereon.
  The SPEAKER pro tempore. Is there objection to the request of the 
gentleman from Missouri?
  There was no objection.
  Mr. CLEAVER. Mr. Speaker, I yield myself such time as I may consume.
  Mr. Speaker, I rise today in support of H.R. 3146, the Securing 
America's Vaccines for Emergencies Act of 2021, introduced by my 
colleague, Mr. French Hill.
  The COVID-19 pandemic has clearly demonstrated that ensuring the 
availability of the essential medical supplies, articles, and equipment 
to fight disease is essential to our national defense. This bill would 
better equip us to respond to the current pandemic, as well as future 
public health emergencies, by amending the Defense Production Act of 
1950, to ensure that the definition of national defense includes the 
availability of medical articles.
  H.R. 3146 strengthens our ability to respond to public health 
emergencies through measures designed to secure the drug supply chain. 
Specifically, the bill requires the development of a strategy on 
securing supply chains for medical articles. This includes reporting to 
Congress on an analysis of existing supply chain vulnerabilities for 
medical articles and recommendations to address these vulnerabilities, 
including measures to diversify supply chains and other efforts to 
mitigate risk, while promoting American competitiveness, scientific 
leadership, and industrial innovation in this area.
  This bill will also provide for investment in supply chain security 
for eligible entities if the President certifies to Congress that such 
an investment is important to meet the national defense needs of the 
United States.
  Mr. Speaker, I thank Mr. Hill for his work in ensuring that we, as a 
country, learn the lessons from this COVID-19 pandemic and are better 
prepared to respond to the next public health emergency because of this 
bill.
  Mr. Speaker, I reserve the balance of my time.
  Mr. HILL. Mr. Speaker, I yield myself such time as I may consume.
  Mr. Speaker, I rise today in support of H.R. 3146, the Securing 
America's Vaccines for Emergencies Act, the SAVE Act. I want to thank 
my friend from California, Juan Vargas, a colleague on the House 
Financial Services Committee, for our collaboration on looking at the 
Defense Production Act--we are going to talk about it today--and how we 
could improve it for better preparing the United States for a global 
pandemic.
  The SAVE Act amends that Defense Production Act to protect medical 
supplies for Americans by bolstering our supply chain during times of 
crisis. The Defense Production Act, as my friend, Mr. Cleaver, noted, 
was first signed into law by President Truman in 1950 in response to a 
shortage of materials during the Korean conflict.
  Designed to incentivize production, avoid inflation, and, as I say, 
boost goods critical for the national defense, the DPA successfully 
brought American manufacturing to the forefront at the battle at hand 
at that time.
  Initially, the Defense Production Act, as you can tell by its name, 
was used in response for military needs, but over time the United 
States Congress has expanded it to other areas considered essential to 
national defense, and those include critical responses to national 
emergencies.
  When President Truman signed the DPA, he shared: It is your fight, 
the fight of all of us, and it can be won only if all of us in the 
fight can fight it together. At that time, he was saying that in 
response to the Korean conflict, but this quote still resonates with us 
now the same way as it did so long ago.
  A little over a year ago, our country faced another nationwide crisis 
that called on the need for the Defense Production Act to be placed in 
the American spotlight. In response to a global health crisis, America 
experienced shortages of necessary medical supplies, basically 
overnight.
  Supply chains were tested like never before, and it became 
increasingly clear that America needed to do something different in 
order to respond to the alarming increase in demand for medical gloves, 
N95 masks, and ventilators.
  In my home State of Arkansas, our hospitals had medical materials 
stacked from floor to ceiling stamped ``Made in China.'' And much of 
those supplies, Mr. Speaker, in the PPE category ended up rejected and 
put in a dumpster because they did not meet the quality standards; they 
were out of compliance.
  Our national and State emergency stockpiles were prepared for a 
localized outbreak, not a national 50-State pandemic. Fortunately, 
President Trump invoked the Defense Production Act, which allowed for 
greater domestic manufacturing of these necessary medical supplies. And 
while that was taking effect, the hospitals and our great Arkansas 
business, academic, and medical community banded together to be able to 
coordinate critical supply purchases, and even locally, manufacture 
badly needed face shields to protect patients and health professionals 
alike.
  Even more alarming than the lack of supplies might be our reliance on 
countries, particularly China, for basic pharmaceutical components. Our 
Nation must develop a strategy to diversify our supply chain to ensure 
that we are not in that same short supply situation in the future. In 
my view, last spring, Mr. Speaker, we were caught without such critical 
planning.
  That is why I introduced the SAVE Act in April of last year when we 
were first responding to these challenges, and I am pleased to have 
reintroduced it this year with my friend and colleague, Congressman 
Vargas. This bill amends the DPA to ensure that medical materials are 
within that Defense Production Act scope.

  While all of us hope that we are nearing the finish line of COVID-19, 
we cannot forget about the shortages that we once faced, because the 
reality is, unfortunately, perhaps likely, this country will face the 
same situation again.
  This bill allows us to be better prepared for that future, whether it 
be in the short, medium, or long run. It will allow us to diversify 
supply chains that are required for our national defense. It will 
permit the United States to be less reliant on foreign countries like 
China for critical PPE or, most importantly, pharmaceutical ingredients 
or other medical products.
  The SAVE Act requires a national strategy and progress reports on the 
diversification of that essential medical supply chain. At the same 
time, it makes explicit that our strategy needs to take into account 
cooperation with our allies. We must maintain a strong trading 
environment that fosters continued innovation. Making critical supply 
chains more resilient doesn't mean closing ourselves off from our 
friends around the world in partnership on these important items.
  Just to cite one example, Mr. Speaker, the Pfizer vaccine against 
COVID-19 consists of 280 components sourced from 86 sites across 19 
countries. International cooperation makes treatments like this 
possible. But we must ensure these items don't fall under the exclusive 
control of an adversary. My legislation will help prevent that.
  Mr. Speaker, I urge all my colleagues on both sides of the aisle to 
support the SAVE Act, and I reserve the balance of my time.
  Mr. CLEAVER. Mr. Speaker, I yield 2 minutes to the gentleman from 
California (Mr. Vargas).
  Mr. VARGAS. Mr. Speaker, I rise today to support my good friend, 
Representative Hill's, SAVE Act, H.R. 3146. As my good friend from 
Arkansas said, I am proud to be the lead cosponsor of this bill. The 
tailored focus on this bill on the supply chain portion of the Defense 
Production Act will help us in future preparedness for public health 
emergencies.

[[Page H2456]]

  Among other things, it requires a detailed plan from the President to 
secure the medical material supply chain. Additionally, it amends the 
DPA, the Defense Production Act, to include medical materials among 
critical materials for which the supply chain must be secured.
  As my good friend knows, we need to be prepared not only for this 
pandemic, unfortunately, for other medical emergencies that may come. 
We have heard that we may be entering an era of pandemics and we must 
be prepared.
  Mr. Speaker, I thank my good friend from Arkansas for his leadership, 
and I urge a ``yes'' vote on this bill's passage.
  Mr. HILL. Mr. Speaker, I yield myself such time as I may consume.
  Mr. Speaker, I thank my friend from California, Mr. Vargas. We will 
be talking about this when we discuss his bill in a few minutes. We 
have collaborated on this, and it is about planning, it is about a 
strategy, it is about not being caught at low tide with no bathing 
suit, and that is what this country needs is a better strategy.
  President Bush warned us of that after he studied this issue when he 
was President. The stockpiles are important. Our FEMA planning is 
important. But our medical supply chain and those critical components 
are critical to the health and safety of our country. It is critical to 
our ability to defend ourselves, and hence, an appropriate amendment to 
the Defense Production Act.
  Mr. Speaker, I have no further speakers, and I urge a ``yes'' vote on 
both sides of the aisle, and I yield back the balance of my time.
  Mr. CLEAVER. Mr. Speaker, I yield myself the balance of my time.
  Mr. Speaker, this time last year we watched as our brave healthcare 
workers struggled all over this country to respond to the mounting 
COVID-19 crisis, often with inadequate personal protective equipment 
and limited medical supplies.
  This bill ensures that we can direct our significant scientific 
innovation and industrial capacity towards ensuring essential medical 
supplies are readily available, and that our supply chains are 
resilient in the face of threats to our collective health and well-
being.
  Mr. Speaker, I would like to thank Mr. Hill for his work on this 
important issue, and I urge all of my colleagues to vote ``yes.'' I 
yield back the balance of my time.
  The SPEAKER pro tempore. The question is on the motion offered by the 
gentleman from Missouri (Mr. Cleaver) that the House suspend the rules 
and pass the bill, H.R. 3146.
  The question was taken; and (two-thirds being in the affirmative) the 
rules were suspended and the bill was passed.
  A motion to reconsider was laid on the table.

                          ____________________