7 U.S.C. § 2143 — Standards and certification process for humane handling, care, treatment, and transportation of animals
submitted 60 years ago by Pub. L. 89-544 to r/title-7-AGRICULTURE · 2,284 words · no verdicts yet
The Secretary must set humane-care standards for animals handled by dealers, research facilities, exhibitors, and transportation providers. Research facilities must use committees, training, reporting, and information procedures, and Federal support may be suspended or revoked for noncompliance. The section also sets transportation certificate, age, and payment rules.
(a) Standards, rules, regulations, and orders.
(1) The Secretary* must issue standards governing the humane handling, care, treatment, and transportation of animals by dealers, research facilities, and exhibitors.
(2) The standards must include minimum requirements—
(A) for handling, housing, feeding, watering, sanitation, ventilation, shelter from extreme weather and temperatures, adequate veterinary care, and separation by species when the Secretary finds separation necessary for humane handling, care, or treatment; and
(B) for exercising dogs, as determined by an attending veterinarian under the Secretary’s general standards, and for giving primates a physical environment adequate to promote their psychological well-being.
(3) For animals in research facilities, the standards must also require—
(A) animal* care, treatment, and experimental practices that minimize pain and distress, including adequate veterinary care and appropriate use of anesthetic, analgesic, or tranquilizing drugs, or euthanasia;
(B) the principal investigator to consider alternatives to any procedure likely to cause pain or distress to an experimental animal;
(C) for any practice that could cause animal pain—
(i) consultation with a doctor of veterinary medicine when planning the procedures;
(ii) use of tranquilizers, analgesics, and anesthetics;
(iii) pre-surgical and post-surgical care by laboratory workers under established veterinary medical and nursing procedures;
(iv) no use of paralytics without anesthesia; and
(v) when scientifically necessary to withhold tranquilizers, anesthesia, analgesia, or euthanasia, withholding them only for the necessary period;
(D) no animal being used in more than one major operative experiment from which it is allowed to recover, except when—
(i) scientifically necessary; or
(ii) the Secretary determines that other special circumstances exist; and
(E) exceptions to the standards being made only when the research protocol specifies them. Each exception must be detailed and explained in the report described in paragraph (7) and filed with the Institutional Animal Committee*.
(4) The Secretary must also issue standards governing transportation in commerce*, and the related handling, care, and treatment, by intermediate handlers, air carriers, and other carriers of animals sent for that transportation by a dealer*, research facility*, exhibitor*, auction-sale operator, other person*, or a United States, State*, or local government department, agency, or instrumentality. The Secretary may issue rules and regulations needed to assure humane treatment during transportation in commerce. These may include requirements about containers, feed, water, rest, ventilation, temperature, and handling.
(5) When issuing and enforcing standards under this section, the Secretary may and must consult experts, including outside consultants when appropriate.
(6)(A) Nothing in this chapter—
(i) except as provided in paragraph (7) of this subsection, authorizes the Secretary to issue rules, regulations, or orders about the design, outlines, or guidelines of actual research or experimentation as the research facility determines them;
(ii) except as provided in paragraph (3)(A) and (C)(ii) through (v) and paragraph (7), authorizes the Secretary to issue rules, regulations, or orders about how the research facility conducts actual research or experimentation; or
(iii) authorizes the Secretary to interrupt actual research or experimentation during an inspection.
(B) No rule, regulation, order, or part of this chapter may be read to require a research facility to disclose publicly or to its Institutional Animal Committee during an inspection any privileged or confidential trade secret or commercial or financial information.
(7)(A) The Secretary must require each research facility, during inspection and at least once a year, to show and report that it follows this chapter and professionally acceptable standards for caring for, treating, and using animals during actual research or experimentation.
(B) To comply with subparagraph (A), a research facility must provide—
(i) information about procedures likely to cause pain or distress to an animal, and assurances showing that the principal investigator considered alternatives;
(ii) assurances satisfactory to the Secretary that the facility follows this section’s standards; and
(iii) an explanation of every deviation from standards issued under this section.
(8) Paragraph (1) does not prevent a State or its political subdivision from issuing additional standards.
(b) Research facility Committee.
(1) The Secretary must require each research facility to establish at least one Committee. The facility’s chief executive officer appoints the Committee. It must have at least three members. The members must be able to assess animal care, treatment, and experimental practices as required by the facility’s needs, and they must represent society’s concerns about the welfare of animal subjects used at the facility.
(A) At least one member must be a doctor of veterinary medicine.
(B) At least one member—
(i) must not be affiliated in any way with the facility other than as a member of the Committee;
(ii) may not be an immediate family member of someone connected with the facility; and
(iii) is intended to represent general community interests in proper animal care and treatment.
(C) If the Committee has more than three members, no more than three may come from the same administrative unit of the facility.
(2) A quorum* is required for every formal Committee action, including inspections under paragraph (3).
(3) At least twice each year, the Committee must inspect all animal study areas and animal facilities of the research facility. As part of each inspection it must review—
(A) practices involving animal pain; and
(B) the animals’ condition, to ensure compliance with this chapter’s requirements for minimizing animal pain and distress.
The Secretary may make an exception to inspecting a study area when animals are studied in their natural environment and the area is too difficult to access easily.
(4)(A) The Committee must file an inspection-certification report for each inspection at the facility. The report must—
(i) be signed by a majority of the Committee members who took part in the inspection;
(ii) report violations of the Secretary’s standards or required assurances, including deficient animal-care or treatment conditions, deviations from originally approved research proposals that harm animal welfare, notices given to the facility about those conditions, and later corrections;
(iii) include any minority views of the Committee; and
(iv) include other information relevant to the Committee’s activities.
(B) The facility must keep the report for at least three years. The Animal and Plant Health Inspection Service and any Federal agency* funding the project may inspect it.
(C) To give the facility a chance to correct deficiencies or deviations found under paragraph (3), the Committee must notify the facility’s administrative representative. If they remain uncorrected after notice and an opportunity to correct them, the Committee must notify the Animal and Plant Health Inspection Service and the funding Federal agency in writing.
(5) Department of Agriculture inspectors may review inspection results during their inspections. They must send Committee inspection records reporting uncorrected deficiencies or deviations to the Animal and Plant Health Inspection Service and to every Federal agency funding the project connected with those deficiencies or deviations.
(c) Federal research facilities. Each Federal research facility* must have a Federal Committee with the same composition and responsibilities described in subsection (b). But the Federal Committee reports deficiencies or deviations to the head of the Federal agency conducting the research, rather than to the Animal and Plant Health Inspection Service. That agency head is responsible for—
(1) all corrective action at the facility; and
(2) granting all exceptions to the inspection protocol.
(d) Training. Each research facility must provide training required by the Secretary for scientists, animal technicians, and other personnel involved in animal care and treatment there. The training must cover—
(1) humane animal maintenance and experimentation;
(2) research or testing methods that minimize or eliminate animal use or limit animal pain or distress;
(3) use of the information service at the National Agricultural Library established under subsection (e); and
(4) ways to report deficiencies in animal care and treatment.
(e) Information service. The Secretary must establish an information service at the National Agricultural Library. Working with the National Library of Medicine, it must provide—
(1) information relevant to employee training;
(2) information that could prevent unintended duplication of animal experiments, as determined by the research facility’s needs; and
(3) information about improved animal-experiment methods, including methods that could—
(A) reduce or replace animal use; and
(B) minimize animal pain and distress, such as anesthetic and analgesic procedures.
(f) Suspension or revocation of Federal support. If a Federal agency funding a research project determines that animal-care, treatment, or practice conditions in a particular project do not comply with standards issued under this chapter, and the Secretary or agency has notified the facility and given it a chance to correct the problem, the agency must suspend or revoke Federal support for the project. A facility that loses support this way has a right to appeal under sections 701 through 706 of title 5.
(f) Veterinary certificate. No dealer, research facility, exhibitor, auction-sale operator, or United States, State, or local government department, agency, or instrumentality may deliver a dog, cat, or additional kind or class of animal designated by the Secretary’s regulation to an intermediate handler* or carrier* for transportation in commerce. Such a person or government entity also may not have the animal received by that handler or carrier for that transportation, unless a licensed veterinarian’s certificate accompanies the animal. The certificate must state that the veterinarian inspected the animal on a specified date no more than 10 days before delivery and that, when inspected, the animal appeared free of infectious disease or physical abnormality that would endanger the animal, other animals, or public health.
The Secretary may make regulatory exceptions to this certificate requirement, under conditions set in the regulations, for animals shipped to research facilities for research, testing, or experimentation that requires animals unable to receive this certification. Intermediate handlers and carriers must keep received certificates as the Secretary’s regulations require, consistent with section 2140.
(g) Age of animals delivered to registered research facilities. No person may deliver a dog, cat, or additional kind or class designated by the Secretary’s regulation to an intermediate handler or carrier for transportation in commerce, except to a registered research facility, if the animal is younger than the age the Secretary sets by regulation. The Secretary must designate additional kinds and classes of animals and may set different ages for particular kinds or classes of dogs, cats, or designated animals when the Secretary finds that doing so is necessary or adequate to assure humane treatment during transportation in commerce.
(h) C.O.D. arrangements. An intermediate handler or carrier transporting an animal in commerce may not take part in an arrangement or practice under which the animal’s cost or transportation cost is paid and collected when the consignee receives the animal. The exception is that the consignor gives a written guarantee to pay transportation charges for an animal not claimed within 48 hours after the consignee is notified that the animal arrived. The guarantee must cover, when necessary, return transportation and enough money to reimburse the carrier for all out-of-pocket costs of caring for, feeding, and storing the animal. This section does not define “dealer,” “research facility,” “exhibitor,” “intermediate handler,” “carrier,” “transportation in commerce,” “professionally acceptable standards,” “principal investigator,” “Institutional Animal Committee,” “animal study area,” “Federal support,” “infectious disease,” “physical abnormality,” “registered research facility,” “consignee,” or “consignor.”
The Secretary* shall promulgate standards to govern the humane handling, care, treatment, and transportation of animals by dealers, research facilities, and exhibitors.
The standards described in paragraph (1) shall include minimum requirements—
for handling, housing, feeding, watering, sanitation, ventilation, shelter from extremes of weather and temperatures, adequate veterinary care, and separation by species where the Secretary finds necessary for humane handling, care, or treatment of animals; and
for exercise of dogs, as determined by an attending veterinarian in accordance with general standards promulgated by the Secretary, and for a physical environment adequate to promote the psychological well-being of primates.
In addition to the requirements under paragraph (2), the standards described in paragraph (1) shall, with respect to animals in research facilities, include requirements—
for animal* care, treatment, and practices in experimental procedures to ensure that animal pain and distress are minimized, including adequate veterinary care with the appropriate use of anesthetic, analgesic, tranquilizing drugs, or euthanasia;
that the principal investigator considers alternatives to any procedure likely to produce pain to or distress in an experimental animal;
in any practice which could cause pain to animals—
that a doctor of veterinary medicine is consulted in the planning of such procedures;
for the use of tranquilizers, analgesics, and anesthetics;
for pre-surgical and post-surgical care by laboratory workers, in accordance with established veterinary medical and nursing procedures;
against the use of paralytics without anesthesia; and
that the withholding of tranquilizers, anesthesia, analgesia, or euthanasia when scientifically necessary shall continue for only the necessary period of time;
that no animal is used in more than one major operative experiment from which it is allowed to recover except in cases of—
scientific necessity; or
other special circumstances as determined by the Secretary; and
that exceptions to such standards may be made only when specified by research protocol and that any such exception shall be detailed and explained in a report outlined under paragraph (7) and filed with the Institutional Animal Committee*.
The Secretary shall also promulgate standards to govern the transportation in commerce*, and the handling, care, and treatment in connection therewith, by intermediate handlers, air carriers, or other carriers, of animals consigned by any dealer*, research facility*, exhibitor*, operator of an auction sale, or other person*, or any department, agency, or instrumentality of the United States or of any State or local government, for transportation in commerce. The Secretary shall have authority to promulgate such rules and regulations as he determines necessary to assure humane treatment of animals in the course of their transportation in commerce including requirements such as those with respect to containers, feed, water, rest, ventilation, temperature, and handling.
In promulgating and enforcing standards established pursuant to this section, the Secretary is authorized and directed to consult experts, including outside consultants where indicated.
Nothing in this chapter—
except as provided in paragraphs 1 (7) of this subsection, shall be construed as authorizing the Secretary to promulgate rules, regulations, or orders with regard to the design, outlines, or guidelines of actual research or experimentation by a research facility as determined by such research facility;
except as provided 2 subparagraphs (A) and (C)(ii) through (v) of paragraph (3) and paragraph (7) of this subsection, shall be construed as authorizing the Secretary to promulgate rules, regulations, or orders with regard to the performance of actual research or experimentation by a research facility as determined by such research facility; and
shall authorize the Secretary, during inspection, to interrupt the conduct of actual research or experimentation.
No rule, regulation, order, or part of this chapter shall be construed to require a research facility to disclose publicly or to the Institutional Animal Committee during its inspection, trade secrets or commercial or financial information which is privileged or confidential.
The Secretary shall require each research facility to show upon inspection, and to report at least annually, that the provisions of this chapter are being followed and that professionally acceptable standards governing the care, treatment, and use of animals are being followed by the research facility during actual research or experimentation.
In complying with subparagraph (A), such research facilities shall provide—
information on procedures likely to produce pain or distress in any animal and assurances demonstrating that the principal investigator considered alternatives to those procedures;
assurances satisfactory to the Secretary that such facility is adhering to the standards described in this section; and
an explanation for any deviation from the standards promulgated under this section.
Paragraph (1) shall not prohibit any State (or a political subdivision of such State) from promulgating standards in addition to those standards promulgated by the Secretary under paragraph (1).
The Secretary shall require that each research facility establish at least one Committee. Each Committee shall be appointed by the chief executive officer of each such research facility and shall be composed of not fewer than three members. Such members shall possess sufficient ability to assess animal care, treatment, and practices in experimental research as determined by the needs of the research facility and shall represent society’s concerns regarding the welfare of animal subjects used at such facility. Of the members of the Committee—
at least one member shall be a doctor of veterinary medicine;
at least one member—
shall not be affiliated in any way with such facility other than as a member of the Committee;
shall not be a member of the immediate family of a person who is affiliated with such facility; and
is intended to provide representation for general community interests in the proper care and treatment of animals; and
in those cases where the Committee consists of more than three members, not more than three members shall be from the same administrative unit of such facility.
A quorum* shall be required for all formal actions of the Committee, including inspections under paragraph (3).
The Committee shall inspect at least semiannually all animal study areas and animal facilities of such research facility and review as part of the inspection—
practices involving pain to animals, and
the condition of animals,
to ensure compliance with the provisions of this chapter to minimize pain and distress to animals. Exceptions to the requirement of inspection of such study areas may be made by the Secretary if animals are studied in their natural environment and the study area is prohibitive to easy access.
The Committee shall file an inspection certification report of each inspection at the research facility. Such report shall—
be signed by a majority of the Committee members involved in the inspection;
include reports of any violation of the standards promulgated, or assurances required, by the Secretary, including any deficient conditions of animal care or treatment, any deviations of research practices from originally approved proposals that adversely affect animal welfare, any notification to the facility regarding such conditions, and any corrections made thereafter;
include any minority views of the Committee; and
include any other information pertinent to the activities of the Committee.
Such report shall remain on file for at least three years at the research facility and shall be available for inspection by the Animal and Plant Health Inspection Service and any funding Federal agency*.
In order to give the research facility an opportunity to correct any deficiencies or deviations discovered by reason of paragraph (3), the Committee shall notify the administrative representative of the research facility of any deficiencies or deviations from the provisions of this chapter. If, after notification and an opportunity for correction, such deficiencies or deviations remain uncorrected, the Committee shall notify (in writing) the Animal and Plant Health Inspection Service and the funding Federal agency of such deficiencies or deviations.
The inspection results shall be available to Department of Agriculture inspectors for review during inspections. Department of Agriculture inspectors shall forward any Committee inspection records which include reports of uncorrected deficiencies or deviations to the Animal and Plant Health Inspection Service and any funding Federal agency of the project with respect to which such uncorrected deficiencies and deviations occurred.
In the case of Federal research facilities, a Federal Committee shall be established and shall have the same composition and responsibilities provided in subsection (b), except that the Federal Committee shall report deficiencies or deviations to the head of the Federal agency conducting the research rather than to the Animal and Plant Health Inspection Service. The head of the Federal agency conducting the research shall be responsible for—
all corrective action to be taken at the facility; and
the granting of all exceptions to inspection protocol.
Each research facility shall provide for the training of scientists, animal technicians, and other personnel involved with animal care and treatment in such facility as required by the Secretary. Such training shall include instruction on—
the humane practice of animal maintenance and experimentation;
research or testing methods that minimize or eliminate the use of animals or limit animal pain or distress;
utilization of the information service at the National Agricultural Library, established under subsection (e); and
methods whereby deficiencies in animal care and treatment should be reported.
The Secretary shall establish an information service at the National Agricultural Library. Such service shall, in cooperation with the National Library of Medicine, provide information—
pertinent to employee training;
which could prevent unintended duplication of animal experimentation as determined by the needs of the research facility; and
on improved methods of animal experimentation, including methods which could—
reduce or replace animal use; and
minimize pain and distress to animals, such as anesthetic and analgesic procedures.
In any case in which a Federal agency funding a research project determines that conditions of animal care, treatment, or practice in a particular project have not been in compliance with standards promulgated under this chapter, despite notification by the Secretary or such Federal agency to the research facility and an opportunity for correction, such agency shall suspend or revoke Federal support for the project. Any research facility losing Federal support as a result of actions taken under the preceding sentence shall have the right of appeal as provided in sections 701 through 706 of title 5.
No dogs or cats, or additional kinds or classes of animals designated by regulation of the Secretary, shall be delivered by any dealer, research facility, exhibitor, operator of an auction sale, or department, agency, or instrumentality of the United States or of any State or local government, to any intermediate handler* or carrier* for transportation in commerce, or received by any such handler or carrier for such transportation from any such person, department, agency, or instrumentality, unless the animal is accompanied by a certificate issued by a veterinarian licensed to practice veterinary medicine, certifying that he inspected the animal on a specified date, which shall not be more than ten days before such delivery, and, when so inspected, the animal appeared free of any infectious disease or physical abnormality which would endanger the animal or animals or other animals or endanger public health: Provided, however, That the Secretary may by regulation provide exceptions to this certification requirement, under such conditions as he may prescribe in the regulations, for animals shipped to research facilities for purposes of research, testing or experimentation requiring animals not eligible for such certification. Such certificates received by the intermediate handlers and the carriers shall be retained by them, as provided by regulations of the Secretary, in accordance with section 2140 of this title.
No dogs or cats, or additional kinds or classes of animals designated by regulation of the Secretary, shall be delivered by any person to any intermediate handler or carrier for transportation in commerce except to registered research facilities if they are less than such age as the Secretary may by regulation prescribe. The Secretary shall designate additional kinds and classes of animals and may prescribe different ages for particular kinds or classes of dogs, cats, or designated animals, for the purposes of this section, when he determines that such action is necessary or adequate to assure their humane treatment in connection with their transportation in commerce.
No intermediate handler or carrier involved in the transportation of any animal in commerce shall participate in any arrangement or engage in any practice under which the cost of such animal or the cost of the transportation of such animal is to be paid and collected upon delivery of the animal to the consignee, unless the consignor guarantees in writing the payment of transportation charges for any animal not claimed within a period of 48 hours after notice to the consignee of arrival of the animal, including, where necessary, both the return transportation charges and an amount sufficient to reimburse the carrier for all out-of-pocket expenses incurred for the care, feeding, and storage of such animals.
Source credit: (Pub. L. 89–544, § 13, Aug. 24, 1966, 80 Stat. 352; Pub. L. 91–579, § 14, Dec. 24, 1970, 84 Stat. 1562; Pub. L. 94–279, §§ 9, 10, Apr. 22, 1976, 90 Stat. 418, 419; Pub. L. 99–198, title XVII, § 1752, Dec. 23, 1985, 99 Stat. 1645.)
- 1966Enacted · Pub. L. 89-544 · 80 Stat. 352
- 1970Amended · Pub. L. 91-579 · 84 Stat. 1562
- 1976Amended · Pub. L. 94-279 · 90 Stat. 418, 419
- 1985Amended · Pub. L. 99-198 · 99 Stat. 1645
A history note hasn’t been published yet. The record shows enactment by Pub. L. 89-544 on 1966-08-24.
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