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15 U.S.C. § 3054 — Jurisdiction of the Commission and the
Federal law — U.S. Code and appendices · legal_authorities
Page 1976
TITLE 15—COMMERCE AND TRADE
§ 3054
1 So in original. Probably should be ‘‘subsection (k)’’.
(2) a list of permitted and prohibited medica-
tions, substances, and methods, including al-
lowable limits of permitted medications, sub-
stances, and methods;
(3) laboratory standards for accreditation
and protocols;
(4) standards for racing surface quality
maintenance;
(5) racetrack safety standards and protocols;
(6) a program for injury and fatality data
analysis;
(7) a program of research and education on
safety, performance, and anti-doping and
medication control;
(8) a description of safety, performance, and
anti-doping and medication control rule viola-
tions applicable to covered horses and covered
persons;
(9) a schedule of civil sanctions for viola-
tions;
(10) a process or procedures for disciplinary
hearings; and
(11) a formula or methodology for deter-
mining assessments described in section 3052(f)
of this title.
(b) Publication and comment
(1) In general
The Commission shall—
(A) publish in the Federal Register each
proposed rule or modification submitted
under subsection (a); and
(B) provide an opportunity for public com-
ment.
(2) Approval required
A proposed rule, or a proposed modification
to a rule, of the Authority shall not take ef-
fect unless the proposed rule or modification
has been approved by the Commission.
(c) Decision on proposed rule or modification to
a rule
(1) In general
Not later than 60 days after the date on
which a proposed rule or modification is pub-
lished in the Federal Register, the Commis-
sion shall approve or disapprove the proposed
rule or modification.
(2) Conditions
The Commission shall approve a proposed
rule or modification if the Commission finds
that the proposed rule or modif
Source: Supplied 2024 U.S. Code historical extraction · 15 U.S.C. § 3054
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Source location: USCODE-2024-title15-chap57A-sec3054.pdf
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Page 1976
TITLE 15—COMMERCE AND TRADE
§ 3054
1 So in original. Probably should be ‘‘subsection (k)’’.
(2) a list of permitted and prohibited medica-
tions, substances, and methods, including al-
lowable limits of permitted medications, sub-
stances, and methods;
(3) laboratory standards for accreditation
and protocols;
(4) standards for racing surface quality
maintenance;
(5) racetrack safety standards and protocols;
(6) a program for injury and fatality data
analysis;
(7) a program of research and education on
safety, performance, and anti-doping and
medication control;
(8) a description of safety, performance, and
anti-doping and medication control rule viola-
tions applicable to covered horses and covered
persons;
(9) a schedule of civil sanctions for viola-
tions;
(10) a process or procedures for disciplinary
hearings; and
(11) a formula or methodology for deter-
mining assessments described in section 3052(f)
of this title.
(b) Publication and comment
(1) In general
The Commission shall—
(A) publish in the Federal Register each
proposed rule or modification submitted
under subsection (a); and
(B) provide an opportunity for public com-
ment.
(2) Approval required
A proposed rule, or a proposed modification
to a rule, of the Authority shall not take ef-
fect unless the proposed rule or modification
has been approved by the Commission.
(c) Decision on proposed rule or modification to
a rule
(1) In general
Not later than 60 days after the date on
which a proposed rule or modification is pub-
lished in the Federal Register, the Commis-
sion shall approve or disapprove the proposed
rule or modification.
(2) Conditions
The Commission shall approve a proposed
rule or modification if the Commission finds
that the proposed rule or modification is con-
sistent with—
(A) this chapter; and
(B) applicable rules approved by the Com-
mission.
(3) Revision of proposed rule or modification
(A) In general
In the case of disapproval of a proposed
rule or modification under this subsection,
not later than 30 days after the issuance of
the disapproval, the Commission shall make
recommendations to the Authority to mod-
ify the proposed rule or modification.
(B) Resubmission
The Authority may resubmit for approval
by the Commission a proposed rule or modi-
fication that incorporates the modifications
recommended under subparagraph (A).
(d) Proposed standards and procedures
(1) In general
The Authority shall submit to the Commis-
sion any proposed rule, standard, or procedure
developed by the Authority to carry out the
horseracing anti-doping and medication con-
trol program or the racetrack safety program.
(2) Notice and comment
The Commission shall publish in the Federal
Register any such proposed rule, standard, or
procedure and provide an opportunity for pub-
lic comment.
(e) Amendment by Commission of rules of au-
thority
The Commission, by rule in accordance with
section 553 of title 5, may abrogate, add to, and
modify the rules of the Authority promulgated
in accordance with this chapter as the Commis-
sion finds necessary or appropriate to ensure the
fair administration of the Authority, to conform
the rules of the Authority to requirements of
this chapter and applicable rules approved by
the Commission, or otherwise in furtherance of
the purposes of this chapter.
(Pub. L. 116–260, div. FF, title XII, § 1204, Dec. 27,
2020, 134 Stat. 3257; Pub. L. 117–328, div. O, title
VII, § 701, Dec. 29, 2022, 136 Stat. 5231.)
Editorial Notes
REFERENCES IN TEXT
This chapter, referred to in subsecs. (c)(2)(A) and (e),
was in the original ‘‘this Act’’ and was translated as
reading ‘‘this title’’, meaning title XII of div. FF of
Pub. L. 116–260, to reflect the probable intent of Con-
gress.
AMENDMENTS
2022—Subsec. (e). Pub. L. 117–328 amended subsec. (e)
generally. Prior to amendment, text read as follows:
‘‘The Commission may adopt an interim final rule, to
take effect immediately, under conditions specified in
section 553(b)(B) of title 5, if the Commission finds that
such a rule is necessary to protect—
‘‘(1) the health and safety of covered horses; or
‘‘(2) the integrity of covered horseraces and wager-
ing on those horseraces.’’
§ 3054. Jurisdiction of the Commission and the
Horseracing Integrity and Safety Authority
(a) In general
Beginning on the program effective date, the
Commission, the Authority, and the anti-doping
and medication control enforcement agency,
each within the scope of their powers and re-
sponsibilities under this chapter, as limited by
subsection (j),1 shall—
(1) implement and enforce the horseracing
anti-doping and medication control program
and the racetrack safety program;
(2) exercise independent and exclusive na-
tional authority over—
(A) the safety, welfare, and integrity of
covered horses, covered persons, and covered
horseraces; and
(B) all horseracing safety, performance,
and anti-doping and medication control mat-
Page 1977
TITLE 15—COMMERCE AND TRADE
§ 3054
2 So in original.
ters for covered horses, covered persons, and
covered horseraces; and
(3) have safety, performance, and anti-
doping and medication control authority over
covered persons similar to such authority of
the State racing commissions before the pro-
gram effective date.
(b) Preemption
The rules of the Authority promulgated in ac-
cordance with this chapter shall preempt any
provision of State law or regulation with respect
to matters within the jurisdiction of the Au-
thority under this chapter, as limited by sub-
section (j).1 Nothing contained in this chapter
shall be construed to limit the authority of the
Commission under any other provision of law.
(c) Duties
(1) In general
The Authority—
(A) shall develop uniform procedures and
rules authorizing—
(i) access to offices, racetrack facilities,
other places of business, books, records,
and personal property of covered persons
that are used in the care, treatment, train-
ing, and racing of covered horses;
(ii) issuance and enforcement of sub-
poenas and subpoenas duces tecum; and
(iii) other investigatory powers of the
nature and scope exercised by State racing
commissions before the program effective
date; and
(B) with respect to an unfair or deceptive
act or practice described in section 3059 of
this title, may recommend that the Commis-
sion commence an enforcement action.
(2) Approval of Commission
The procedures and rules developed under
paragraph (1)(A) shall be subject to approval
by the Commission in accordance with section
3053 of this title.
(d) Registration of covered persons with Author-
ity
(1) In general
As a condition of participating in covered
races and in the care, ownership, treatment,
and training of covered horses, a covered per-
son shall register with the Authority in ac-
cordance with rules promulgated by the Au-
thority and approved by the Commission in
accordance with section 3053 of this title.
(2) Agreement with respect to Authority rules,
standards, and procedures
Registration under this subsection shall in-
clude an agreement by the covered person to
be subject to and comply with the rules, stand-
ards, and procedures developed and approved
under subsection (c).
(3) Cooperation
A covered person registered under this sub-
section shall, at all times—
(A) cooperate with the Commission, the
Authority, the anti-doping and medication
control enforcement agency, and any respec-
tive designee, during any civil investigation;
and
(B) respond truthfully and completely to
the best of the knowledge of the covered per-
son if questioned by the Commission, the
Authority, the anti-doping and medication
control enforcement agency, or any respec-
tive designee.
(4) Failure to comply
Any failure of a covered person to comply
with this subsection shall be a violation of
section 3057(a)(2)(G) of this title.
(e) Enforcement of programs
(1) Anti-doping and medication control en-
forcement agency
(A) Agreement with USADA
The Authority shall seek to enter into an
agreement with the United States Anti-
Doping Agency under which the Agency acts
as the anti-doping and medication control
enforcement agency under this chapter for
services consistent with the horseracing
anti-doping and medication control pro-
gram.
(B) Agreement with other entity
If the Authority and the United States
Anti-Doping Agency are unable to enter into
the agreement described in subparagraph
(A), the Authority shall enter into an agree-
ment with an entity that is nationally rec-
ognized as being a medication regulation
agency equal in qualification to the United
States Anti-Doping Agency to act as the
anti-doping and medication control enforce-
ment agency under this chapter for services
consistent with the horseracing anti-doping
and medication control program.
(C) Negotiations
Any negotiations under this paragraph
shall be conducted in good faith and de-
signed to achieve efficient, effective best
practices for anti-doping and medication
control and enforcement on commercially
reasonable terms.
(D) Elements of agreement
Any agreement under this paragraph shall
include a description of the scope of work,
performance metrics, reporting obligations,
and budgets of the United States Anti-
Doping Agency while acting as the anti-
doping and medication control enforcement
agency under this chapter, as well as a pro-
vision for the revision of the agreement to
increase in the scope of work as provided for
in subsection (k),2 and any other matter the
Authority considers appropriate.
(E) Duties and powers of enforcement agency
The anti-doping and medication control
enforcement agency under an agreement
under this paragraph shall—
(i) serve as the independent anti-doping
and medication control enforcement orga-
nization for covered horses, covered per-
sons,
and
covered
horseraces,
imple-
menting the anti-doping and medication
control program on behalf of the Author-
ity;
Page 1978
TITLE 15—COMMERCE AND TRADE
§ 3054
(ii) ensure that covered horses and cov-
ered persons are deterred from using or ad-
ministering medications, substances, and
methods in violation of the rules estab-
lished in accordance with this chapter;
(iii) implement anti-doping education,
research, testing, compliance and adju-
dication programs designed to prevent cov-
ered persons and covered horses from using
or administering medications, substances,
and methods in violation of the rules es-
tablished in accordance with this chapter;
(iv) exercise the powers specified in sec-
tion 3055(c)(4) of this title in accordance
with that section; and
(v) implement and undertake any other
responsibilities specified in the agreement.
(F) Term and extension
(i) Term of initial agreement
The initial agreement entered into by
the Authority under this paragraph shall
be in effect for the 5-year period beginning
on the program effective date.
(ii) Extension
At the end of the 5-year period described
in clause (i), the Authority may—
(I) extend the term of the initial agree-
ment under this paragraph for such addi-
tional term as is provided by the rules of
the Authority and consistent with this
chapter; or
(II) enter into an agreement meeting
the requirements of this paragraph with
an entity described by subparagraph (B)
for such term as is provided by such
rules and consistent with this chapter.
(2) Agreements for enforcement by State rac-
ing commissions
(A) State racing commissions
(i) Racetrack safety program
The Authority may enter into agree-
ments with State racing commissions for
services consistent with the enforcement
of the racetrack safety program.
(ii) Anti-doping and medication control
program
The anti-doping and medication control
enforcement agency may enter into agree-
ments with State racing commissions for
services consistent with the enforcement
of the anti-doping and medication control
program.
(B) Elements of agreements
Any agreement under this paragraph shall
include a description of the scope of work,
performance metrics, reporting obligations,
budgets, and any other matter the Authority
considers appropriate.
(3) Enforcement of standards
The Authority may coordinate with State
racing commissions and other State regu-
latory agencies to monitor and enforce race-
track compliance with the standards devel-
oped under paragraphs (1) and (2) of section
3056(c) of this title.
(f) Procedures with respect to rules of Authority
(1) Anti-doping and medication control
(A) In general
Recommendations for rules regarding anti-
doping and medication control shall be de-
veloped in accordance with section 3055 of
this title.
(B) Consultation
The anti-doping and medication control
enforcement agency shall consult with the
anti-doping and medication control standing
committee and the Board of the Authority
on all anti-doping and medication control
rules of the Authority.
(2) Racetrack safety
Recommendations for rules regarding race-
track safety shall be developed by the race-
track safety standing committee of the Au-
thority.
(g) Issuance of guidance
(1) The Authority may issue guidance that—
(A) sets forth—
(i) an interpretation of an existing rule,
standard, or procedure of the Authority; or
(ii) a policy or practice with respect to the
administration or enforcement of such an
existing rule, standard, or procedure; and
(B) relates solely to—
(i) the administration of the Authority; or
(ii) any other matter, as specified by the
Commission, by rule, consistent with the
public interest and the purposes of this sub-
section.
(2) Submittal to Commission
The Authority shall submit to the Commis-
sion any guidance issued under paragraph (1).
(3) Immediate effect
Guidance issued under paragraph (1) shall
take effect on the date on which the guidance
is submitted to the Commission under para-
graph (2).
(h) Subpoena and investigatory authority
The Authority shall have subpoena and inves-
tigatory authority with respect to civil viola-
tions committed under its jurisdiction.
(i) Civil penalties
The Authority shall develop a list of civil pen-
alties with respect to the enforcement of rules
for covered persons and covered horseraces
under its jurisdiction.
(j) Civil actions
(1) In general
In addition to civil sanctions imposed under
section 3057 of this title, the Authority may
commence a civil action against a covered per-
son or racetrack that has engaged, is engaged,
or is about to engage, in acts or practices con-
stituting a violation of this chapter or any
rule established under this chapter in the
proper district court of the United States, the
United States District Court for the District
of Columbia, or the United States courts of
any territory or other place subject to the ju-
risdiction of the United States, to enjoin such
Page 1979
TITLE 15—COMMERCE AND TRADE
§ 3055
1 So in original. Probably should be ‘‘section 3054(l)’’.
acts or practices, to enforce any civil sanc-
tions imposed under that section, and for all
other relief to which the Authority may be en-
titled.
(2) Injunctions and restraining orders
With respect to a civil action commenced
under paragraph (1), upon a proper showing, a
permanent or temporary injunction or re-
straining order shall be granted without bond.
(k) Limitations on authority
(1) Prospective application
The jurisdiction and authority of the Au-
thority and the Commission with respect to
the horseracing anti-doping and medication
control program and the racetrack safety pro-
gram shall be prospective only.
(2) Previous matters
(A) In general
The Authority and the Commission may
not investigate, prosecute, adjudicate, or pe-
nalize conduct in violation of the horse-
racing anti-doping and medication control
program and the racetrack safety program
that occurs before the program effective
date.
(B) State racing commission
With respect to conduct described in sub-
paragraph (A), the applicable State racing
commission shall retain authority until the
final resolution of the matter.
(3) Other laws unaffected
This chapter shall not be construed to mod-
ify, impair or restrict the operation of the
general laws or regulations, as may be amend-
ed from time to time, of the United States, the
States and their political subdivisions relating
to criminal conduct, cruelty to animals, mat-
ters unrelated to antidoping, medication con-
trol and racetrack and racing safety of cov-
ered horses and covered races, and the use of
medication in human participants in covered
races.
(l) Election for other breed coverage under chap-
ter
(1) In general
A State racing commission or a breed gov-
erning organization for a breed of horses other
than Thoroughbred horses may elect to have
such breed be covered by this chapter by the
filing of a designated election form and subse-
quent approval by the Authority. A State rac-
ing commission may elect to have a breed cov-
ered by this chapter for the applicable State
only.
(2) Election conditional on funding mechanism
A commission or organization may not
make an election under paragraph (1) unless
the commission or organization has in place a
mechanism to provide sufficient funds to cover
the costs of the administration of this chapter
with respect to the horses that will be covered
by this chapter as a result of the election.
(3) Apportionment
The Authority shall apportion costs de-
scribed in paragraph (2) in connection with an
election under paragraph (1) fairly among all
impacted segments of the horseracing indus-
try, subject to approval by the Commission in
accordance with section 3053 of this title. Such
apportionment may not provide for the alloca-
tion of costs or funds among breeds of horses.
(Pub. L. 116–260, div. FF, title XII, § 1205, Dec. 27,
2020, 134 Stat. 3259.)
Editorial Notes
REFERENCES IN TEXT
This chapter, referred to in subsecs. (a), (b), (e)(1),
(j)(1), (k)(3), and (l)(1), (2), was in the original ‘‘this
Act’’ and was translated as reading ‘‘this title’’, mean-
ing title XII of div. FF of Pub. L. 116–260, to reflect the
probable intent of Congress.
§ 3055. Horseracing anti-doping and medication
control program
(a) Program required
(1) In general
Not later than the program effective date,
and after notice and an opportunity for public
comment in accordance with section 3053 of
this title, the Authority shall establish a
horseracing anti-doping and medication con-
trol program applicable to all covered horses,
covered persons, and covered horseraces in ac-
cordance with the registration of covered per-
sons under section 3054(d) of this title.
(2) Consideration of other breeds
In developing the horseracing anti-doping
and medication control program with respect
to a breed of horse that is made subject to this
chapter by election of a State racing commis-
sion or the breed governing organization for
such horse under section 3054(k) 1 of this title,
the Authority shall consider the unique char-
acteristics of such breed.
(b) Considerations in development of program
In developing the horseracing anti-doping and
medication control program, the Authority
shall take into consideration the following:
(1) Covered horses should compete only when
they are free from the influence of medica-
tions, other foreign substances, and methods
that affect their performance.
(2) Covered horses that are injured or un-
sound should not train or participate in cov-
ered races, and the use of medications, other
foreign substances, and treatment methods
that mask or deaden pain in order to allow in-
jured or unsound horses to train or race should
be prohibited.
(3) Rules, standards, procedures, and proto-
cols regulating medication and treatment
methods for covered horses and covered races
should be uniform and uniformly administered
nationally.
(4) To the extent consistent with this chap-
ter, consideration should be given to inter-
national anti-doping and medication control
standards of the International Federation of
Horseracing Authorities and the Principles of
Veterinary Medical Ethics of the American
Veterinary Medical Association.
Cross-references
Connections may be documented source relationships, shared citations or nearby passages. Each explains its basis; a connection alone does not establish applicability to your situation.
Federal law — U.S. Code and appendices · legal_authorities
**(a) In general** Beginning on the program effective date, the Commission, the Authority, and the anti-doping and medication control enforcement agency, each within the scope of their powers and responsibilities under this chapter, as limited by subsection (j),11 So in original. Probably should be “subsection (k)”. shall—
(1) implement and enforce the horseracing anti-doping and medication control program and the racetrack safety program;
(2) exercise independent and exclusive national authority over—
(A) the safety, welfare, and integrity of covered horses, covered persons, and covered horseraces; and
(B) all horseracing safety, performance, and anti-doping and medication control matters for covered horses, covered persons, and covered horseraces; and
(3) have safety, performance, and anti-doping and medication control authority over covered persons similar to such authority of the State racing commissions before the program effective date.
**(b) Preemption** The rules of the Authority promulgated in accordance with this chapter shall preempt any provision of State law or regulation with respect to matters within the jurisdiction of the Authority under this chapter, as limited by subsection (j).1 Nothing contained in this chapter shall be construed to limit the authority of the Commission under any other provision of law.
**(c) Duties**
(1) **In general** — The Authority—
(A) shall develop uniform procedures and rules authorizing—
(i) access to offices, racetrack facilities, other places of business, books, records, and personal property of covered persons that are used in the care, treatment, training, and racing of covered horses;
(ii) issuance and enforcement of subpoenas and subpoenas duces tecum; and
(iii) other investigatory powers
Source: Supplied U.S. Code snapshot — release unconfirmed · 15 U.S.C. § 3054
Stored review status: release_metadata_unconfirmed. Same stored citation; legal effect and authority still require review.