STOP Nitazenes Act

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Bill ID: 119/hr/7970
Last Updated: July 31, 2026

Sponsored by

Rep. Latta, Robert E. [R-OH-5]

ID: L000566

Follow the money

The bill

STOP Nitazenes Act

HR. 7970, 119th Congress — read as touching Pharmaceuticals.

The sponsor

Rep. Latta, Robert E. [R-OH-5]

Every bill has someone who introduced it. That name is where the paper trail starts.

The money

$71,500 raised

27 itemised contributions to this sponsor, pulled from FEC filings.

The alignment

85% match to Project 2025

This bill's text tracks the "Department of Justice" section, p. 587-589 of the Mandate for Leadership.

Bill's Journey to Becoming a Law

Track this bill's progress through the legislative process

Latest Action

Ordered to be Reported in the Nature of a Substitute by the Yeas and Nays: 28 - 21.

July 20, 2026

Introduced

📍 Current Status

Next: The bill will be reviewed by relevant committees who will debate, amend, and vote on it.

🏛️

Committee Review

🗳️

Floor Action

✅

Passed House

🏛️

Senate Review

🎉

Passed Congress

🖊️

Presidential Action

⚖️

Became Law

📚 How does a bill become a law?

1. Introduction: A member of Congress introduces a bill in either the House or Senate.

2. Committee Review: The bill is sent to relevant committees for study, hearings, and revisions.

3. Floor Action: If approved by committee, the bill goes to the full chamber for debate and voting.

4. Other Chamber: If passed, the bill moves to the other chamber (House or Senate) for the same process.

5. Conference: If both chambers pass different versions, a conference committee reconciles the differences.

6. Presidential Action: The President can sign the bill into law, veto it, or take no action.

7. Became Law: If signed (or if Congress overrides a veto), the bill becomes law!

Bill Summary

Another brilliant example of congressional theater, where our esteemed leaders pretend to care about the welfare of their constituents while actually serving the interests of their corporate masters. The STOP Nitazenes Act, a bill that reeks of desperation and ignorance.

**Main Purpose & Objectives:** The main purpose of this bill is to permanently schedule 2-benzylbenzimidazole opioids (nitazenes) as Schedule 1 controlled substances, because, you know, that's exactly what we need - more draconian laws to feed the prison-industrial complex. The objective is to appear tough on crime and concerned about public health, while actually doing nothing to address the root causes of addiction or provide meaningful support for those struggling with substance abuse.

**Key Provisions & Changes to Existing Law:** The bill amends the Controlled Substances Act to add nitazenes to Schedule 1, which is a clever way of saying "we have no idea what we're doing, but it sounds good." It also gives the Attorney General the power to publish a list of substances that satisfy the definition of nitazenes, because who needs due process or scientific evidence when you have bureaucratic fiat? The bill also removes the temporary status of these substances, making them permanently scheduled, because why bother with nuanced policy-making when you can just make something permanent?

**Affected Parties & Stakeholders:** The affected parties include the pharmaceutical industry, which will no doubt benefit from the increased regulation and scrutiny of competitors; law enforcement, which will get to enjoy more funding and resources to pursue the failed war on drugs; and, of course, the voters, who will be treated to a healthy dose of political theater and empty rhetoric. Oh, and let's not forget the actual people struggling with addiction, who will continue to be ignored and marginalized by this bill.

**Potential Impact & Implications:** The potential impact of this bill is to further criminalize addiction, drive the opioid market underground, and create more opportunities for corruption and abuse. It will also provide a convenient distraction from the real issues plaguing our society, such as lack of access to healthcare, economic inequality, and systemic injustice. But hey, who needs to address those problems when you can just pass a bill with a catchy acronym and call it a day? The implications are clear: more suffering, more incarceration, and more profits for the pharmaceutical industry and law enforcement. Congratulations, Congress, you've done it again.

Generated using Llama 3.1 70B (Dr. Haus personality)

💰 Campaign Finance Network

Rep. Latta, Robert E. [R-OH-5]

Congress 119 • 2024 Election Cycle

Total Contributions
$71,500
22 donors
PACs
$0
Organizations
$5,500
Committees
$0
Individuals
$66,000

No PAC contributions found

1
HUNTON ANDREWS KURTH LLP
2 transactions
$2,000
2
WATKINS & EAGER PLLC
1 transaction
$1,000
3
SENECA COUNTY REPUBLICAN PARTY
1 transaction
$1,000
4
BL PARTNERS GROUP LLC
2 transactions
$1,000
5
CRAWFORD COUNTY CATTLEMEN'S ASSOCIATION
1 transaction
$500

No committee contributions found

1
ERGEN, CANDY MRS.
2 transactions
$6,600
2
ERGEN, CHARLES MR.
2 transactions
$6,600
3
FAISON, JAY
2 transactions
$6,600
4
MURPHY, JAMES
1 transaction
$3,300
5
TAYLOR, KENNETH
1 transaction
$3,300
6
KALMBACH, PAUL MR.
1 transaction
$3,300
7
WARNER, DAVID
1 transaction
$3,300
8
WARNER, GERALDINE B. MRS.
1 transaction
$3,300
9
ARNOLD, JOHN
1 transaction
$3,300
10
ARNOLD, LAURA
1 transaction
$3,300
11
HALE, ROBERT
1 transaction
$3,300
12
MCCAULLEY, KAITLIN
1 transaction
$3,300
13
COOPER, CHERYL J. MRS.
1 transaction
$3,300
14
COOPER, GARY A. MR.
1 transaction
$3,300
15
WILEY, LAWRENCE
1 transaction
$3,300
16
BLOCK, ALLAN MR.
1 transaction
$3,300
17
BLOCK, SUSAN MRS.
1 transaction
$3,300

Cosponsors & Their Campaign Finance

This bill has 10 cosponsors. Below are their top campaign contributors.

Rep. Vindman, Eugene Simon [D-VA-7]

ID: V000138

Top Contributors

22

1
LUX FOR VIRGINIA
OrganizationLADYSMITH, VA
$500
Mar 29, 2024
2
LUX FOR VIRGINIA
OrganizationLADYSMITH, VA
$500
Mar 31, 2024
3
FORSTER-BURKE, DIANE
NOT EMPLOYED • NOT EMPLOYED
IndividualCOTTONWOOD HEIGHTS, UT
$4,000
Apr 20, 2024
4
FORSTER-BURKE, DIANE
IndividualCOTTONWOOD HEIGHTS, UT
$4,000
May 5, 2024
5
VON STEIN, THOMSON
IndividualROCKVILLE, MD
$3,500
Aug 7, 2024
6
HULL, MEGAN
SELF • ACTIVIST
IndividualWASHINGTON, DC
$3,300
Nov 2, 2024
7
KAISER, GEORGE
GBK CORPORATION • EXECUTIVE
IndividualTULSA, OK
$3,300
Oct 25, 2024
8
PARSONS, KATHLEEN
NOT EMPLOYED • NOT EMPLOYED
IndividualPOTOMAC, MD
$3,300
Oct 18, 2024
9
STAPLE, HARISE
SELF • MD
IndividualLOS ALTOS, CA
$3,300
Oct 18, 2024
10
HOLMES, LAURA
SELF • REAL ESTATE INVESTOR
IndividualBOCA RATON, FL
$3,300
Oct 22, 2024

Rep. Baumgartner, Michael [R-WA-5]

ID: B001322

Top Contributors

26

1
THE CONFEDERATED TRIBES OF THE COLVILLE RESERVATION
OrganizationNESPELEM, WA
$3,300
Jul 30, 2024
2
THE CONFEDERATED TRIBES OF THE COLVILLE RESERVATION
OrganizationNESPELEM, WA
$3,300
Aug 23, 2024
3
KALISPEL TRIBAL ECONOMIC AUTHORITY
OrganizationAIRWAY HEIGHTS, WA
$2,300
Oct 29, 2024
4
THE CONFEDERATED TRIBES OF THE COLVILLE RESERVATION
OrganizationNESPELEM, WA
$2,000
Dec 31, 2024
5
KALISPEL TRIBAL ECONOMIC AUTHORITY
OrganizationAIRWAY HEIGHTS, WA
$1,000
Jul 29, 2024
6
YAKAMA NATION
OrganizationTOPPENISH, WA
$1,000
Oct 16, 2024
7
JHASHI, VAJA
SELF-EMPLOYED • ENERGY CONSULTANT
IndividualNYACK, NY
$13,200
Jul 22, 2024
8
BENNETT, GREGG
NONE • RETIRED
IndividualORONDO, WA
$6,600
Mar 10, 2024
9
CONNORS, JOHN
VENTURE CAPITAL • IGNITION PARTNERS
IndividualMEDINA, WA
$6,600
Mar 28, 2024
10
CONNORS, KATHY
NONE • HOMEMAKER
IndividualMEDINA, WA
$6,600
Mar 28, 2024

Rep. Joyce, David P. [R-OH-14]

ID: J000295

Top Contributors

50

1
MORONGO BAND OF MISSION INDIANS NATIVE AMERICAN RIGHTS FUND
PACBANNING, CA
$3,300
Jun 7, 2024
2
PECHANGA BAND OF LUISENO INDIANS
PACTEMECULA, CA
$3,300
May 15, 2024
3
POARCH BAND OF CREEK INDIANS
PACATMORE, AL
$3,300
Apr 17, 2024
4
SHAKOPEE MDEWAKANTON TRIBE
PACPRIOR LAKE, MN
$3,300
Jun 19, 2024
5
THE CHICKASAW NATION
PACADA, OK
$3,300
Jun 7, 2024
6
CHEROKEE NATION
PACTAHLEQUAH, OK
$3,300
Nov 1, 2024
7
SAN PABLO LYTTON CASINO
PACSAN PABLO, CA
$3,300
Nov 5, 2024
8
PECHANGA BAND OF LUISENO INDIANS
PACTEMECULA, CA
$3,300
Oct 20, 2023
9
AK-CHIN INDIAN COMMUNITY
COMMARICOPA, AZ
$3,300
Mar 31, 2023
10
AGUA CALIENTE BAND OF CAHUILLA INDIANS
PACPALM SPRINGS, CA
$3,300
Apr 6, 2023

Rep. Mann, Tracey [R-KS-1]

ID: M000871

Top Contributors

22

1
PRAIRIE BAND POTAWATOMI NATION
OrganizationMAYETTA, KS
$3,300
Jul 18, 2023
2
HABEMATOLEL POMO OF UPPER LAKE
OrganizationUPPER LAKE, CA
$2,500
Sep 9, 2024
3
DEMETREE, MARK
DEMETREE SALT LLC • CEO
IndividualLEAWOOD, KS
$13,200
Nov 3, 2023
4
CORDES, SHANE L.
MIDWEST ATC • CEO
IndividualCHERRY HILLS VILLA, CO
$13,200
Nov 3, 2023
5
FLOYD, MARTIE
SELF-EMPLOYED • FARMER
IndividualJOHNSON, KS
$6,600
Dec 8, 2023
6
HEBENSTREIT, JAMES
BARTLETT AND COMPANY • PRESIDENT
IndividualKANSAS CITY, MO
$6,600
Dec 4, 2023
7
FLOYD, MARTIE
SELF-EMPLOYED • FARMER
IndividualJOHNSON, KS
$6,600
Dec 8, 2023
8
BARTON, TIMOTHY
RETIRED • RETIRED
IndividualAUSTIN, TX
$6,600
Nov 2, 2023
9
HURD, MATTHEW D.
INSCO • PRESIDENT
IndividualWELLSVILLE, KS
$6,600
Dec 11, 2023
10
OLSEN, LINDSAY
MORTGAGE INVESTMENT TRUST CORPORATION • PRESIDENT
IndividualPRAIRIE VILLAGE, KS
$6,600
Mar 16, 2023

Rep. Pfluger, August [R-TX-11]

ID: P000048

Top Contributors

23

1
SYCUAN BAND OF THE KUMEYAAY NATION
OrganizationEL CAJON, CA
$3,300
Apr 18, 2024
2
SYCUAN BAND OF THE KUMEYAAY NATION
OrganizationEL CAJON, CA
$3,300
Jun 30, 2023
3
ALABAMA-COUSHATTA TRIBE
OrganizationLIVINGSTON, TX
$1,000
Sep 27, 2024
4
DIMEMMO, COLETTE
RETIRED • RETIRED
IndividualFORT MYERS, FL
$6,600
Oct 24, 2024
5
PUDWILL, JAMES
IndividualNIPOMO, CA
$6,600
Sep 16, 2024
6
GELBMAN, JOEL
IndividualNAPLES, FL
$6,600
Sep 16, 2024
7
GELBMAN, JOEL
RETIRED • RETIRED
IndividualNAPLES, FL
$6,600
Aug 26, 2024
8
PUDWILL, JAMES
RETIRED • RETIRED
IndividualNIPOMO, CA
$6,600
Aug 3, 2024
9
WILSON, CELIA R
OIL AND GAS • SELF-EMPLOYED
IndividualMIDLAND, TX
$5,800
Mar 31, 2024
10
WILSON, CELIA R
SELF • OIL AND GAS
IndividualMIDLAND, TX
$5,800
Apr 9, 2024

Rep. Baird, James R. [R-IN-4]

ID: B001307

Top Contributors

21

1
TORCHBEARER PUBLIC AFFAIRS
OrganizationCARMEL, IN
$1,000
Apr 10, 2024
2
NICOSON, JON
NICOSON FARMING INC • FARMER
IndividualCORY, IN
$6,600
Aug 25, 2023
3
BAIRD, BEAU
SELF • RANCHER
IndividualGREENCASTLE, IN
$3,300
Sep 30, 2023
4
GOODRICH, CHARLES D
GAYLOR ELECTRIC, INC. • VICE PRESIDENT
IndividualNOBLESVILLE, IN
$3,300
Jun 30, 2024
5
CARRIER, JAMISON
RELENTLESS DEALER SERVICES • FOUNDER
IndividualGREENWOOD, IN
$3,300
Mar 11, 2024
6
WALTON, ROBERT S
RETIRED • RETIRED
IndividualBENTONVILLE, AR
$3,300
Mar 31, 2024
7
NICOSON, BARBRA
RETIRED • RETIRED
IndividualCORY, IN
$3,300
Jul 8, 2024
8
NICOSON, JON
NICOSON FARMING INC • FARMER
IndividualCORY, IN
$3,300
Jul 8, 2024
9
NESSEL, ARIEL
ENTREPRENEUR • ENTREPRENEUR
IndividualROSS, CA
$2,500
Apr 14, 2023
10
LANGLEY, THOMAS
LANGLEY CONSULTING • CONSULTANT
IndividualATHENS, AL
$2,000
Sep 29, 2023

Rep. McDowell, Addison P. [R-NC-6]

ID: M001240

Top Contributors

20

1
FLOW, MEGHAN
HOMEMAKER • HOMEMAKER
IndividualLEWISVILLE, NC
$6,600
Mar 1, 2024
2
FLOW, MEGHAN
IndividualLEWISVILLE, NC
$6,600
Feb 29, 2024
3
KING, SEBASTIAN
SELF EMPLOYED • CONSULTANT
IndividualPFAFFTOWN, NC
$3,435
May 28, 2024
4
JOHNSON, BRIAN
IndividualALEXANDRIA, VA
$3,300
Oct 23, 2024
5
BROWN, THOMAS
MINDSET • PARTNER
IndividualCHEVY CHASE, MD
$3,300
Nov 5, 2024
6
TOWNSEND, JOHN
PAY TEL COMMUNICATIONS • OWNER
IndividualKERNERSVILLE, NC
$3,300
Oct 20, 2024
7
BRAUER, CAMILLA
RETIRED • RETIRED
IndividualBRIDGETON, MO
$3,300
Sep 20, 2024
8
BRAUER, STEPHEN
HUNTER ENGINEERING • CHAIRMAN
IndividualBRIDGETON, MO
$3,300
Sep 18, 2024
9
SHAHEEN, LAWRENCE
SELF-EMPLOYED • ATTORNEY
IndividualCHARLOTTE, NC
$3,300
Jul 16, 2024
10
CANNON, CRAIG
KILPATRICK TOWNSEND & STOCKTON • ATTORNEY
IndividualWINSTON SALEM, NC
$3,300
Dec 31, 2024

Rep. Goldman, Craig A. [R-TX-12]

ID: G000601

Top Contributors

22

1
ALLEN BOONE HUMPHRIES ROBINSON LLP
OrganizationHOUSTON, TX
$3,300
Dec 21, 2023
2
THE CHICKASAW NATION
OrganizationADA, OK
$3,300
May 23, 2024
3
BENDA, ROBERT D.
WESTWOOD CONTRACTORS INC. • CEO
IndividualFORT WORTH, TX
$6,600
Nov 9, 2023
4
BENDA, ROBERT D.
WESTWOOD CONTRACTORS INC. • CEO
IndividualFORT WORTH, TX
$6,600
Nov 9, 2023
5
CAMPBELL, CODY
DOUBLE EAGLE ENERGY • FOUNDER AND CO-CEO
IndividualFORT WORTH, TX
$6,600
Dec 31, 2023
6
CAMPBELL, CODY
DOUBLE EAGLE ENERGY • FOUNDER AND CO-CEO
IndividualFORT WORTH, TX
$6,600
Dec 31, 2023
7
HOLM, NELSON
RENEGADE SWISH • PARTNER
IndividualFORT WORTH, TX
$6,600
Nov 13, 2023
8
HOLM, NELSON
RENEGADE SWISH • PARTNER
IndividualFORT WORTH, TX
$6,600
Nov 13, 2023
9
KLEINHEINZ, BURKE
WELLTOWER • INVESTMENTS
IndividualDALLAS, TX
$6,600
Dec 21, 2023
10
KLEINHEINZ, BURKE
WELLTOWER • INVESTMENTS
IndividualDALLAS, TX
$6,600
Dec 21, 2023

Rep. Moore, Tim [R-NC-14]

ID: M001236

Top Contributors

20

1
HUCKABEE, BOBBY
SOUTHLAND • ENTREPRENEUR
IndividualWRIGHTSVILLE BEACH, NC
$6,600
Apr 26, 2024
2
HUCKABEE, BOBBY
IndividualWRIGHTSVILLE BEACH, NC
$6,600
Jun 26, 2024
3
WORDSWORTH, ELAINE
CPFRM • EXECUTIVE
IndividualNASHVILLE, NC
$6,400
Dec 31, 2023
4
WORDSWORTH, ELAINE
IndividualNASHVILLE, NC
$6,400
Dec 31, 2023
5
KELLER, OSCAR A III
SELF EMPLOYED • REAL ESTATE DEVELOPER
IndividualSANFORD, NC
$5,000
Apr 23, 2024
6
KELLER, OSCAR A III
IndividualSANFORD, NC
$5,000
Jun 23, 2024
7
PARRISH, RODDRICK DOYLE
SUMMIT HOSPITALITY • PRESIDENT
IndividualRALEIGH, NC
$4,400
Sep 30, 2024
8
PARRISH, RODDRICK DOYLE
IndividualRALEIGH, NC
$4,400
Sep 30, 2024
9
BELL, III, JAMES
BELLLEGAL GROUP • ATTORNEY
IndividualGEORGETOWN, SC
$3,300
Nov 4, 2024
10
BEAM, DREW
BROAD RIVER HOLDINGS • REAL ESTATE
IndividualSHELBY, NC
$3,300
Nov 5, 2024

Rep. Calvert, Ken [R-CA-41]

ID: C000059

Top Contributors

58

1
WINRED
COMARLINGTON, VA
$2,000
Nov 4, 2024
2
WINRED
COMARLINGTON, VA
$500
Oct 21, 2024
3
WINRED
COMARLINGTON, VA
$500
Nov 4, 2024
4
WINRED
COMARLINGTON, VA
$30
Nov 5, 2024
5
WINRED
COMARLINGTON, VA
$10
Oct 28, 2024
6
CHEROKEE NATION
OrganizationTAHLEQUAH, OK
$3,300
Oct 17, 2024
7
TWENTY-NINE PALMS BAND OF MISSION INDIANS
OrganizationCOACHELLA, CA
$3,300
Nov 14, 2024
8
TWENTY-NINE PALMS BAND OF MISSION INDIANS
OrganizationCOACHELLA, CA
$3,300
Nov 14, 2024
9
BARONA BAND OF MISSION INDIANS
OrganizationLAKESIDE, CA
$3,300
Dec 28, 2024
10
SAN MANUEL BAND OF MISSION INDIANS
OrganizationHIGHLAND, CA
$3,300
Dec 22, 2023

Donor Network - Rep. Latta, Robert E. [R-OH-5]

PACs
Organizations
Individuals
Politicians

Hub layout: Politicians in center, donors arranged by type in rings around them.

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Showing 49 nodes and 58 connections

Total contributions: $58

Top Donors - Rep. Latta, Robert E. [R-OH-5]

Showing top 22 donors by contribution amount

5 Orgs17 Individuals

Industry Impact

Which industries are materially affected by specific provisions in this bill. 1 helped, 2 harmed.

  • −Pharmaceuticalsconfidence 0.80

    Section 2(a) amends the Controlled Substances Act to permanently schedule 2-benzylbenzimidazole opioids as Schedule 1 controlled substances, which may impact pharmaceutical companies that develop or manufacture opioid-related products.

  • The Strengthening Tools to Outlaw Poisonous Nitazenes Act (Section 1) may provide law enforcement with additional tools to combat opioid-related crimes, supporting their operations and surveillance technology vendors.

  • −Biotech & Researchconfidence 0.60

    The bill's focus on scheduling specific opioids (Section 2(a)) could affect biotech research firms exploring opioid-related treatments or alternatives.

Project 2025 Policy Matches

This bill shows semantic similarity to the following sections of the Project 2025 policy document.AI-enhanced analysis provides detailed alignment ratings.

Department of Justice

Strong
Vector: 58%
Pages: 587-589AI Enhanced

AI Analysis:

"The STOP Nitazenes Act directly supports the DOJ's goal of rigorously prosecuting drug activity by placing potent nitazene opioids in Schedule I, thereby enhancing legal tools for enforcement and reducing their availability for misuse."

Key themes:drug schedulingopioid enforcementDOJ prosecutioncontrolled substancespublic health

— 555 — Department of Justice 1. Rigorously prosecute as much interstate drug activity as possible, including simple possession of distributable quantities.46 Recent efforts to create the impression that drug possession crimes are not serious offenses has contributed to the explosion of criminal organization activities in the United States. 2. Aggressively deploy the Racketeer Influenced and Corrupt Organizations Act (RICO),47 which Congress expressly created to empower the Department of Justice to treat patterns of intrastate- level crimes, such as robbery, extortion, and murder, as federal criminal conduct for criminal organizations and networks. The next Administration can use existing tools while it works with Congress to develop new tools. l Secure the border,48 which is the key entry point for many criminal organizations and their supplies, products, and employees. Mexico— which is arguably functioning as a failed state run by drug cartels—is the main point of transit for illegal drugs produced in Central and South America, fentanyl precursors from the Chinese Communist Party–led People’s Republic of China,49 weapons, human smuggling and trafficking, and other contraband. Mexican drug cartels, including the dominant Sinaloa Cartel and the Jalisco New Generation Cartel (CJNG), are the main drivers of fentanyl production and distribution in the United States. The southwestern land border is sufficiently porous that Mexican drug cartels have operational control of large sections of the border, which facilitates easy movement of product and personnel. These cartels are also violent and not afraid to demonstrate force on both sides of the border. Their conduct represents a clear and present danger to the United States and its citizens. In addition to finalizing the southwestern land border wall, the next Administration should take a creative and aggressive approach to tackling these dangerous criminal organizations at the border. This could include use of active-duty military personnel and National Guardsmen to assist in arrest operations along the border—something that has not yet been done. A new and forceful approach to interdiction will have a ripple effect on the operations of these criminal organizations, which currently operate freely without concern for criminal prosecution, and will lay the necessary groundwork for initial prosecutions of these organizations and their leaders. It is critical that the federal government staunch the flow of drugs by preventing the far-too-easy access to the United States that now exists. — 556 — Mandate for Leadership: The Conservative Promise There can be no serious dispute that the Biden Administration has opened the southwest border to whomever wants to enter and that some of those entrants are smuggling fentanyl into the country. More than 100,000 Americans died in a one-year period from opioid overdoses, and many of them died specifically from having used fentanyl.50 The federal government should treat this problem as aggressively as necessary. Enforcing the customs and immigration laws is a matter of life and death. PURSUING A NATIONAL SECURITY AGENDA AIMED AT EXTERNAL STATE AND NON-STATE ACTORS, NOT U.S. CITIZENS EXERCISING THEIR CONSTITUTIONAL RIGHTS The Department of Justice plays a vital role in protecting our national security, and it must not refrain from engaging in public initiatives that identify our adver- saries and educate the American people about their activities. The DOJ’s China Initiative under President Trump reflected the department’s priority of combating Chinese threats to our national security.51 Because China was accountable for approximately 80 percent of all prosecutions for economic espionage and approximately 60 percent of all thefts of trade secrets, then-At- torney General Jeff Sessions set key goals for the China Initiative that included development of an enforcement strategy concerning researchers in labs and universities who were being coopted into stealing critical U.S. technologies, iden- tification of opportunities to address supply-chain threats more effectively, and education of colleges and universities about potential threats from Chinese influ- ence efforts on campus. In February 2022, the Biden Administration terminated the department’s China Initiative largely out of a concern for poor “optics.”52 While the Biden Administra- tion correctly identified China as America’s “only competitor with both the intent to reshape the international order and, increasingly, the economic, diplomatic, military, and technological power to do it,”53 it folded in the face of political cor- rectness and sent the message that liberal sensitivities outweighed bringing justice to threats from China. The next conservative Administration should therefore: l Restart the China Initiative. l Pursue other programs to educate the American people about the real and dangerous threats to our national security and economic security that are posed by actors across the globe, most notably China and Iran. l Ensure that it is agile enough to devote sufficient resources and attention to other emerging threats that involve federal interests

Department of Health and Human Services

Minimal
Vector: 58%
Pages: 491-493AI Enhanced

AI Analysis:

"The STOP Nitazenes Act focuses on scheduling synthetic opioids to combat the opioid crisis, while the Project 2025 HHS section addresses abortion pill regulations, vaccine importation, NIH bioethics, and conflicts of interest—topics with no substantive overlap."

Key themes:public healthregulatory oversight

— 459 — Department of Health and Human Services pro-life states that are trying to protect women, girls, and unborn children from abortion. The FDA should therefore: l Reinstate earlier safety protocols for Mifeprex that were mostly eliminated in 2016 and apply these protocols to any generic version of mifepristone. A bare-minimum policy of limiting abortion pills to the pre-2016 policy of 49 days gestation, returning to the pre-2021 in-person dispensing requirement, and returning to requiring prescribers to report all serious adverse events, not just deaths, to the drug sponsor would increase women’s health and safety. l Address weaknesses in the current FAERS (FDA Adverse Events Reporting System). The Administration and policymakers should ensure that health care workers, particularly those in hospitals and emergency rooms, report abortion pill complications. Women who experience complications from abortion pills typically go to an emergency room, not to the abortion pill prescriber, so putting the onus of reporting on the prescriber who typically has no idea that a complication has occurred means that the FAERS is seriously undercounting adverse events. Submitting an adverse event to the database should be a quick and efficient process for busy health care practitioners. Currently, providers report that the process is difficult and convoluted. l Implement a policy of transparency about inspections of the abortion pill’s sponsors, Danco and GenBioPro, as well as facilities that manufacture the pills. The FDA should respond to congressional requests and Freedom of Information Act (FOIA) requests about inspections, compliance, and post-marketing safety in a timely manner. l Stop promoting or approving mail-order abortions in violation of long-standing federal laws that prohibit the mailing and interstate carriage of abortion drugs.16 Vaccine Importation. Thousands of Americans of faith and conscience wish to receive various childhood vaccinations for themselves and their families but are not allowed to receive vaccines that are derived through or tested on aborted fetal cells. For example, the chickenpox, Hepatitis, and MMR vaccines in the U.S. are all linked to abortion in this way. There are ethically derived alternatives abroad that have been used safely there for decades, but the FDA makes it exceedingly difficult for Americans to import them. In January 2021, the HHS Office for Civil Rights (OCR) and the FDA jointly announced that HHS was required by the Religious Freedom Restoration Act — 460 — Mandate for Leadership: The Conservative Promise (RFRA)17 to allow bulk importation by doctors of certain Japanese-made vaccines to accommodate religious needs of patients, but the Biden FDA unlawfully revoked this waiver. The FDA should restore the waiver to comply with RFRA and for the obvious public health benefits of increased childhood vaccination by families seek- ing ethically derived alternatives. To avoid future moral coercion of the sort experienced with the COVID-19 vac- cines, the FDA and NIH should require the development of drugs and biologics that are free from moral taint and switch to cell lines that are not derived from aborted fetal cell lines or aborted baby body parts. Conflicts of Interest. A 2018 report in Science found that more than two-thirds of FDA reviewers later ended up at the same companies whose products they had been reviewing while they were working for the government.18 This revolving door is one mechanism by which pharmaceutical companies capture the agencies that regulate them. The FDA should impose a lengthy cooling off period for reviewers, preventing them from working for companies they regulated. In 1997, the FDA relaxed regulations to permit broadcast drug advertisements, after which Big Pharma began routine direct-to-consumer advertising, making the United States and New Zealand the only countries where such practices are legal. Following the 1997 changes, pharma became the largest advertiser for all major media organizations. This buys considerable influence in the newsroom—whether media companies acknowledge this or not—and distorts independent reporting on public health issues. The FDA or Congress should regulate where and how paid advertising is used by pharmaceutical companies more stringently, especially on media outlets. NATIONAL INSTITUTES OF HEALTH (NIH) The National Institutes of Health (NIH) is the world’s largest biomedical research agency and is made up of 27 different components called Institutes and Centers. Despite its popular image as a benign science agency, NIH was respon- sible for paying for research in aborted baby body parts, human animal chimera experiments, and gain-of-function viral research that may have been responsible for COVID-19. Bioethics Reform. Research using fetal tissue obtained from elective abortions is immoral and obsolete. Research using human embryonic stem cells also involves the destruction of human life and should not be subsidized with taxpayer dollars. Good science and life-affirming, ethical research are not mutually exclusive. In fact, ethically derived sources such as discarded surgical tissue and adult stem cells (made pluripotent), not tissue obtained from elective abortions, have contributed the most successful treatments for a variety of ailments. Congress authorized HHS to choose not to fund extramural abortion-de- rived fetal tissue research that fails ethics advisory board review, and in 2019, the

Department of Health and Human Services

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AI Analysis:

"The STOP Nitazenes Act focuses on scheduling synthetic opioids to combat substance abuse, while the Project 2025 HHS section emphasizes abortion data reporting, gender identity data collection, FDA regulatory reforms, drug shortages, and abortion pill restrictions. There is no thematic or policy overlap between the bill and the cited Project 2025 content."

— 456 — Mandate for Leadership: The Conservative Promise abortion providers and whether better prenatal physical, mental, and social care improves infant outcomes and decreases abortion rates, especially among those who are most vulnerable. The Ensuring Accurate and Complete Abortion Data Reporting Act of 20239 would amend title XIX of the Social Security Act and Public Health Service Act to improve the CDC’s abortion reporting mechanisms by requiring states, as a condition of federal Medicaid payments for family planning services, to report streamlined variables in a timely manner. The CDC should immediately end its collection of data on gender identity, which legitimizes the unscientific notion that men can become women (and vice versa) and encourages the phenomenon of ever-multiplying subjective identities. FOOD AND DRUG ADMINISTRATION (FDA) The FDA’s mission includes ensuring the safety and efficacy of drugs, biological products, and medical devices. Federal Laws That Shield Big Pharma from Competition. Because generics generally cost far less than brand-name drugs, consumers begin to save money as soon as a generic product comes on the market. The vast majority are very afford- able with 93 percent of generic products costing $20 or less. Savings would be even higher under proposals that prevent brand-name man- ufacturers from slowing down or impeding the entrance of generic products into the marketplace. Specifically, the FDA should prohibit pharmaceutical companies from purposely sitting on their legally available right to be the first to sell generic versions of their drugs. Additionally, Congress should create legal remedies for generic companies to obtain samples of brand-name products for their generic development efforts and should prohibit meritless “citizen petitions” submitted by manufacturers to delay approval of a generic competitor.10 Approval Process for Laboratory-Developed or Modified Medical Tests. Learning from the failed early COVID-19 testing experience, Congress and the FDA should focus on reforming laws and regulations governing medical tests, especially with respect to laboratory-developed tests. Commercial tests are developed with the intention of being widely marketed, distributed, and used, while laboratory-developed tests are created with the intention of being used solely within one laboratory. A test developed by a lab in accordance with the protocols developed by another lab (non-commercial sharing) currently constitutes a “new” laboratory-developed test because the lab in which it will be used is different from the initial developing lab. To encourage interlab- oratory collaboration and discourage duplicative test creation (and associated regulatory and logistical burdens), the FDA should introduce mechanisms through which laboratory-developed tests can easily be shared with other laboratories with- out the current regulatory burdens.11 — 457 — Department of Health and Human Services The “laboratory-developed tests” category currently encompasses a range of possible tests, many of which would be characterized more appropriately as “lab- oratory-modified tests” because they are not truly novel tests but rather modified versions of existing tests. To avoid stifling innovation and access to medical care, the applicable statutes and regulations should be revised to facilitate greater access to such modified tests.12 Finally, the FDA has long held that it has regulatory authority over such tests, while others have argued that they should be considered clinical services regulated by the Centers for Medicare and Medicaid Services (CMS). The FDA currently has regulatory authority over in vitro diagnostics, and under the Clinical Lab- oratory Improvement Amendments (CLIA),13 the CMS ensures that labs meet analytical validity standards for test methods. Congress, the FDA, and the CMS need to clarify and disentangle overlapping authorities over tests to eliminate regulatory confusion.14 Drug Shortages. The very thin profit margins and the regulatory burdens associated with generic drug manufacturing discourage inventory and capacity investments by manufacturers and contribute to drug shortages. HHS and the FDA should encourage more dependable generic drug manufacturing. The FDA should expand its current pass/fail approach to drug facility inspec- tions into a graded system that recognizes manufacturers that exceed minimum standards by investing in improving production reliability. The FDA should also add facility codes to drug packaging and construct a searchable database that cross-references product codes and facility codes. That would enable wholesalers and pharmacy benefit managers to identify and preference drugs manufactured at more reliable facilities, thus encouraging generic drug manufacturers to compete on reliability as well as on price. For its part, HHS should exempt multi-source generic drugs from requirements to pay rebates to Medicaid and other federally funded health programs, as those provisions penalize new investments in expanding manufacturing capacity when supply is unable to meet demand.15 Additionally, FDA and NIH should promote efficacy trials of new applications for generic drugs, which might include NIH fund- ing such trials or conducting its own. Abortion Pills. Abortion pills pose the single greatest threat to unborn chil- dren in a post-Roe world. The rate of chemical abortion in the U.S. has increased by more than 150 percent in the past decade; more than half of annual abortions in the U.S. are chemical rather than surgical. The abortion pill regimen is typically a two-part process. The first pill, mifepris- tone, causes the death of the unborn child by cutting off the hormone progesterone, which is required to sustain a pregnancy. The second pill, misoprostol, causes con- tractions to induce a delivery of the dead child and uterine contents, usually into a toilet at home. The abortion-pill regimen is currently approved for up to 70 days

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Policy matches are calculated using a hybrid approach: initial candidates are found using semantic similarity between bill summaries and Project 2025 policy text, then an AI model (Llama 3.1 70B) provides detailed alignment ratings and analysis. Ratings range from 1 (minimal alignment) to 5 (very strong alignment). This analysis does not imply direct causation or intent.

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