Main Content

Overiew

Institutional Animal Care and Use Committee

All faculty and students using live vertebrate animals — whether for research or teaching, on or off campus — must submit a Research Review Request to the Institutional Animal Care and Use Committee (IACUC). He or she must obtain approval before beginning the research. The IACUC page will provide further information on how to submit an application for a study and what to do once it is approved.

Animal Research Ethics Training

Research involving animals must abide by the federal regulations protecting animal subjects (Animal Welfare Act/Animal Welfare Regulations). It is the responsibility of the investigators to become familiar with these regulations and ensure that all studies conducted at ACU abide by these policies. In addition, all research protocols submitted to the IACUC will require online training for every member of the research team. The Animal Research Ethics Training page will provide further information on these regulations and training.

Ethical Requirements

  1. When live animals are used in research, there must be a reasonable expectation that such utilization will contribute to the enhancement of human or animal health, the advancement of knowledge or the good of society. The benefits of the research must clearly outweigh any pain, discomfort and distress experienced by the animals.
  2. It is the responsibility of the investigator to consider the source of the animal and to ensure that all animals used for experimental purposes are lawfully acquired.
  3. The investigator has an ethical obligation to seek the least painful techniques feasible to obtain the protocol objectives. The pain, discomfort and distress should be monitored using behavioral signs based on the normal behavior pattern of the species under study.
  4. Appropriate anesthetics, analgesics and tranquilizers must be used if the procedure will cause more than slight momentary pain or distress to the animal. This pertains to pain or discomfort that may be experienced during, as well as after, the procedure, until such time when the pain is either alleviated or reduced to an acceptable tolerance level. If the use of anesthetics and/or analgesics will compromise the scientific validity of the experiment, the deletion of these drugs must be based on scientific fact or experimental data which can be referenced.
  5. Physical restraints should not be used on awake animals. If such a procedure is necessary, the animal should be conditioned to the restraint prior to beginning the experiment. Prolonged physical restraint of awake animals should be avoided.
  6. Adequate post surgical/procedural care for the animal is the responsibility of the investigator.
  7. Any proposed use of euthanasia must be consistent with recommendations of the American Veterinary Medical Association (AVMA) panel on euthanasia. Such measures include a quick, painless death for the animal. If the animals will not be euthanized at the completion of the experiment, it is the responsibility of the investigator to assure that the final disposition of the animal is both humane and acceptable.
  8. The committee shall review any areas or situations not covered by these standards.

Submission Instructions

Download and complete the appropriate forms in the ORSP Canvas Classroom. You can learn how to access this through our Forms page. Please use the names already assigned to the files and submit all forms as Word documents (with the exception of the Signature and Assurances page which may be submitted as a pdf). Please do not compile individual forms into a single document.

Submit all forms to orsp@acu.edu and include in the subject line the following information:

  • Type of Review being Requested: NS for New Study, AMD for Amendment, CR for Continuing Review, UAE for Unanticipated Event, NC for Non-Compliance, IA for Inactivation, CS for Consult, AWR for Animal Welfare Report
  • Protocol ID assigned to your study during the initial application (for requests other than new studies)
  • Principal Investigator’s Last Name
  • The words ANIMAL

For example: NS Johnson ANIMAL

AMD 15-123ANM Jones ANIMAL
CR 15-124ANM Williams ANIMAL

Please not that all submissions must be accompanied by a signed assurance form. This form MUST be reviewed and signed by an ACU faculty person who agrees to take responsibility for the assurances listed therein.

Submitting a New Study

While not all activities require USDA compliance, it is advised that all activities be submitted for determination and confirmation of compliance. In addition, it is expected that all ethical standards will be followed even in activities that are exempt from USDA compliance.

Please complete the appropriate application below and any other requested items and submit to orsp@acu.edu per the submission instructions.

Forms

  • Animal Research Request, Observation
  • Animal Research Request, Wildlife
  • Animal Research Request, NonWildlife/Captive
  • Signature and Assurance Form, Animal

Also attached, if applicable:

  • Training Certificates
  • Copies of Permits

Study Details and Expectations

Any and all proposed changes to a study, no matter how minor (including changes to personnel, methodology or numbers), must receive prior approval by the IACUC before being implemented.

Significant changes that require IACUC review include those involving new procedures, changes in pain/distress categories, change in primary personnel (e.g., PI), or changes in species.

Minor administrative changes, such as changes in non-essential personnel or contact information, may be submitted for administrative approval by the IACUC Office.

Minor increases in animal numbers may be administratively approved when the request is no more than 10% of the initial request and a satisfactory justification for the increase is provided. The IACUC chair may make this determination. At any time, the chair may determine that the request requires IACUC review.

For the above amendments, an amendment request form may be submitted detailing the request.

Certain changes may be approved by Veterinary Verification and Consultation (VVC). Such requests must not involve new procedures, but may involve minor changes to already approved procedures, such as the frequency, duration or number of procedures performed; the type or dose of medication used; or the method of euthanasia. To request a VVC, the researchers should complete a consultation form and submit it to orsp@acu.edu. The request will be sent to the veterinarian who will determine if the requested change is permissible under VVC, conduct the consult, and either approve the request, recommend revisions, or defer the decision to the IACUC.

Please complete the forms below and any other requested items and submit to orsp@acu.edu per the submission instructions.

Forms

  • Amendment Request Form, Animal
  • Signature and Assurance Form, Animal
  • All revised forms with all changes made in track changes

Also attach, if applicable:

  • NIH Training Certificates for any new team members
  • Any new forms identified in the Amendment Request Form
  • Unanticipated Event, Noncompliance Form, Animals, (if the amendment request is due to a problem)

All studies that were previously approved and that continue beyond one year must undergo continuing review once per year until inactivated. Studies with a high degree of risk may be reviewed more frequently at the IACUC’s discretion. Your original approval letter from the IACUC provides information about when your study expires and must be re-reviewed. Please submit the continuing review materials 30-60 days prior to expiration to orsp@acu.edu per the submission instructions.

If your study expires before you obtain re-approval, you must halt all research activity on that protocol until approval is received or unless the IACUC determines it is in the interest of animal safety to continue.

If you have completed all research activities on a particular protocol, please inactivate that protocol.

Forms

  • Continuing Review Form, Animals
  • Signature and Assurance Form, Animals

Also attach, if applicable:

  • NIH Training Certificates for any new team members
  • Unanticipated Events, Noncompliance Form, Animals

All studies that were previously approved must be inactivated upon completion of the study and records stored by the investigator for at least three years. Inactivation should be completed when animal use is complete and end points have been reached. Please submit the inactivation materials at least 30 days prior to expiration to orsp@acu.edu per the submission instructions.

Forms

  • Inactivation Request Form, Animals
  • Signature and Assurance Form, Animals

Also attach, if applicable:

  • Unanticipated Events, Noncompliance Form, Animals

If you have an unexpected event that potentially increases the risk profile of the study or otherwise affects the welfare of the animals or the research personnel, then you should self-report this to the IACUC. Unanticipated problems that are serious (e.g., increases pain and distress, mortality or morbidity to animals beyond that originally described in the protocol) should be reported within seven days of learning of the event. If it is an emergency, please contact the veterinarian as soon as possible. Other unanticipated problems should be reported within 14 days of learning of the event.

In addition, any deviation from the approved protocol, no matter how small, must be reported to the IACUC using the same timeline as above. If the reported deviation is a permanent change, it must be accompanied by an amendment request form.

If you need to report an unanticipated problem or an event of noncompliance, please complete the forms below and any other requested items and submit to orsp@acu.edu per the submission instructions.

Forms

  • Unanticipated Event, Noncompliance Form, Animals
  • Signature and Assurance Form, Animals

Also attach, if applicable:

  • Amendment Form, Animals
  • Inactivation Form, Animals

If you have reason to suspect that any research personnel is violating the Animal Welfare Act/Animal Welfare Regulations, or any other standard ethical guidelines related to animal research, you may report these concerns to the ORSP/IACUC Office. Any persons with concerns regarding animal welfare may bring these concerns in writing or in person to the IACUC chair. Matters that cannot be resolved by a simple conversation are brought to the full committee for discussion and resolution. Concerns may be reported anonymously, and there will be no repercussions for personnel reporting policy violations. Whistleblower protections are posted in the Employee Handbook (421).

If you need to report an animal welfare concern, please complete the form below. You may email this form to orsp@acu.edu or to the IACUC chair directly at megan.roth@acu.edu. You may also hand deliver this form to the ORSP Office in 320 Hardin Administration Building. You may send the form anonymously through campus mail to ACU Box 29103 c/o Megan Roth. Finally, you may place an anonymous phone call to the ORSP Office at 674-2885.

Forms

Reporting Welfare Concern Animals

If you have questions about a proposed study or require guidance regarding USDA regulations, you may request an IACUC consult.

If you have questions regarding veterinary matters, such as appropriate dosing for drug treatments, standard veterinary practices or procedures, requests for procedural training, etc., you may request a veterinary consult.

In addition, certain changes to an active protocol may be approved by Veterinary Verification and Consultation (VVC). Such requests must not involve new procedures, but may involve minor changes to already approved procedures, such as the frequency, duration or number of procedures performed; the type or dose of medication used; or the method of euthanasia. To request a VVC, the researchers should complete a consultation form and submit it to orsp@acu.edu. The request will be sent to the veterinarian who will determine if the requested change is permissible under VVC, conduct the consult, and either approve the request, recommend revisions or defer the decision to the IACUC.

If you wish to request a consult with either the IACUC or the veterinarian, please complete the consultation form and submit to orsp@acu.edu.

Forms

Consultation Form, Animals

Thank you to Bryn Mawr University for generously sharing their Animal Care Policy for adaptation by Abilene Christian University

I.  Applicability of Policy

This policy is applicable to all research, research training, experimentation, biological testing and related activities, and teaching, hereinafter referred to as activities, involving live, vertebrate animals at this institution or involving the institution’s faculty, staff or students when represented by the institution. This policy covers only those facilities and components listed below.

II.  Institutional Commitment

A. This institution will comply with all applicable provisions of the Animal Welfare Act (AWA)/Animal Welfare Regulations (AWR) and other federal statutes and regulations relating to animals, when applicable and required by law.

B. This institution acknowledges and accepts responsibility for the care and use of animals involved in activities covered by this policy. As partial fulfillment of this responsibility, this institution will ensure that all individuals involved in the care and use of animals for the purposes defined in this policy understand their individual and collective responsibilities for compliance with this policy as well as all other applicable laws and regulations pertaining to animal care and use.

C. This institution agrees to ensure that all performance sites engaged in activities involving live vertebrate animals have Institutional Animal Care and Use Committee (IACUC) approval, in accordance with AWA/AWR.

D. Additional guidance may be sought from the following resources, as appropriate:

a. “U.S. Government Principles for the Utilization and Care of Vertebrate Animals Used in Testing, Research and Training.”

b. “Guide for the Care and Use of Laboratory Animals”  (“The  Guide”)

c. “Guide for the Care and Use of Agricultural Animals in Research and Teaching” (“The Ag Guide”).

d. American Society of Mammalogists Animal Care and Use Guidelines

e. Ornithological Council Guidelines to the Use of Wild Birds in Research

f. American Society of Ichthyologists and Herpetologists Guidelines to the Use of Fishes in Research; Guidelines to the Use of Amphibians and Reptiles in Research

III. Institutional Program for Animal Care and Use

A. The lines of authority and responsibility for administering the program and ensuring compliance with this policy are:

orsp-animal-care-policy-diagram

B.  The qualifications, authority and percent of time contributed by veterinarian(s) who will participate in the program are as follows:

Dr. Stephanie Carle, D.V.M. is the veterinarian who participates in the IACUC, contributing time as needed to the functions of the IACUC.  Her qualifications are as follows:

Dr. Carle is the full-time veterinarian for the Abilene Zoo, demonstrating experience with a variety of animals of captivity and wildlife. She has past experience serving in an IACUC role.

We have established a relationship with Dr. Carle that permits us to avail ourselves of her services on an “as needed” basis rather than in terms of some fixed percentage of her time. Dr. Carle has delegated program authority and responsibility for the institution’s animal care and use program and has access to all animals and protocols.

C. This institution has established an Institutional Animal Care and Use Committee (IACUC), is properly appointed in accordance with the AWA/AWR and is qualified through the experience and expertise of its members to oversee the institution’s animal care and use program and facilities. The IACUC consists of at least three members, and its membership meets the compositional requirements set forth in the AWA/AWR.

D. The IACUC will:

a. Review at least once every six months the institution’s program for humane care and use of animals, using the documents outlined in II as a basis for evaluation. The IACUC procedures for conducting semiannual program reviews are as follows:

The chair calls a meeting at least every six months. At least two members must be in attendance for review to take place. Prior to the meeting, the chair reviews the evaluation checklist to ensure it is complete and accurately reflects the current animal program, and distributes the checklist and any other supporting materials to the committee. At the review meetings, guests from relevant departments and the Office of Risk Management may be invited to report on all activities involving animals, training and/or occupational health and safety. All elements of the checklist are reviewed and discussed. Records are provided to IACUC members as needed to determine the status of the program. Deficiencies are noted, timelines for correction discussed and recommendations for the IO noted. The chair follows up on any matters of concern with relevant campus personnel.

b. While no laboratory animals will be housed by this institution, agricultural facilities housing animals for agricultural purposes will be reviewed at the time of semi-annual review. At this time, the ACU Farm will provide assurance that no agricultural animals will be used for purposes other than agricultural uses and/or agricultural research, as defined by the AWA/AWRs.

c. Prepare reports of the IACUC evaluations according to AWA/AWR and submit the reports to the Institutional Official (IO). The IACUC procedures for developing reports and submitting them to the Institutional Official are as follows:

Detailed minutes of review meetings and evaluations are taken by the chair and transcribed for the report. As appropriate, the report is circulated electronically to members of the IACUC for majority signature prior to submission to the Institutional Official and includes any applicable minority views. Any departures from the AWA and the documents outlined in IIE, as appropriate, are included in the report submitted to the Institutional Official. Departures are identified as significant or minor, and a plan for correction is included.

Such departures are discussed with the researcher involved and corrections requested. The IACUC chair follows up on the corrections that are made. The chair reports any deficiencies in the program or facilities to the IO. The chair also meets in person with the IO to review progress toward remediation of deficiencies. When significant deficiencies are not addressed according to the plan, this will be reported to USDA, when required, within 15 business days of the deadline.

d. Review concerns involving the care and use of animals at the institution. The IACUC procedures for reviewing concerns are as follows:

Any matters arising regarding specific concerns are discussed by the IACUC. In general, responses to concerns by students or others not involved in any animal research (such as students interested in animal rights issues) are addressed by one-on-one meetings with the department chair or departmental representatives. A written report is submitted to the institutional official about the IACUC findings and recommendations.

Any persons with concerns regarding animal welfare may bring these concerns in writing or in person to the IACUC chair. Matters that cannot be resolved by a simple conversation are brought to the full committee for discussion and resolution. Concerns may be reported anonymously, and there will be no repercussions for personnel reporting policy violations.

This policy is posted on the Sponsored Research Office website at www.acu.edu/academics/orsp/non-human-research/animal-research.html. In addition, instructions for reporting concerns regarding animal welfare are also available on that site.

e. Make written recommendations to the Institutional Official regarding any aspect of the institution’s animal program or personnel training. The procedures for making recommendations to the Institutional Official are as follows:

Recommendations are developed by the committee and are drafted by the chair. All proposals are reviewed and approved by members of the committee, who are free to propose alternative suggestions until consensus is reached. These proposals are sent to the Institutional Official. The chair also provides liaison with relevant campus offices to assure that recommendations are carried out.

f. In accordance with the AWA/AWR, the IACUC shall review and approve, require modifications in (to secure approval), or withhold approval of covered activities related to the care and use of animals. The IACUC procedures for protocol review, are as follows:

Protocols are submitted on a standardized form, consistent with policy guidelines, for all non-agricultural research and teaching activities involving the use of live vertebrate animals. Protocols are circulated electronically to all committee members and given at least one week to call for a full board meeting. If no call is made, the protocol will be sent to a single voting IACUC member for designated review. This member will be selected by the IACUC Chair. If called to full board, the protocol will be discussed at a meeting of a quorum of voting members. All voting members may ask questions and propose changes as appropriate. The committee conducts voice votes at meetings, with decisions made by simple majority of voting members in attendance. Possible outcomes include “Approval,” “Approval with Clarifications or Modifications” or “Approval Withheld.” The chair communicates to the investigator in writing either approval, request for clarification prior to approval, request for specific changes or denial of approval. In the case of requested revisions, the committee will determine at the full board meeting whether revisions can be confirmed by a designated voting member or whether the protocol needs to return to full board meeting. The decision to allow designated review of revisions must be unanimous. The designated reviewer will be assigned by the IACUC chair.

Full board reviews may, on occasion, take place electronically, according to guidelines in NIH Notice #NOT-OD-06-052. A meeting may be conducted by real-time conference call or by videoconference with a quorum of IACUC members to confirm the vote. Members must be given all necessary materials in advance and be able to interact and vote in real time.

If a designated review is assigned, the IACUC member is generally given a two-week period to review and make a decision. Decisions may include “Approval” or “Approval with Clarifications or Modifications.” However, a designated reviewer may not withhold approval. In such a case, the protocol must be discussed at a full board meeting.

Guidelines for determining designated review vs. full board:

It is recommended that full board meetings be called for studies involving a high degree or potential for pain, distress or harm. Such studies may be those involving, but not limited to, survival surgery, radiation sickness, tumor inducement, toxicology or infectious disease. Designated review may be appropriate for studies involving, but not limited to, non-survival surgery, tissue collection, antibody production, telemetry or behavioral observation, when appropriate steps are taken to minimize pain and distress.

Committee members with conflicts of interest (for example, those submitting research protocols for review) must recuse themselves from all deliberations on the protocol, other than to answer questions. They may not vote to approve any research activities for which there is a conflict of interest. Consultants may attend meetings and contribute to discussion; however, these individuals do not count toward quorum and may not vote.

No activities covered under this policy may begin until IACUC approval is granted.

g. Procedures to review and approve, require modifications in (to secure approval) or withhold approval of proposed changes regarding the use of animals in ongoing activities as set forth in the AWA. The IACUC procedures for reviewing proposed significant changes in ongoing research projects are similar to those outlined in Section D-6.

Significant changes that require IACUC review include those involving new procedures, changes in pain/distress categories, change in primary personnel (e.g., PI) or changes in species.

Minor administrative changes, such as changes in non-essential personnel or contact information, may be submitted for administrative approval by the IACUC Office.

Minor increases in animal numbers may be administratively approved when the request is no more than 10% of the initial request and a satisfactory justification for the increase is provided. The IACUC chair may make this determination. At any time, the chair may determine that the request requires IACUC review.

Certain changes may be approved by Veterinary Verification and Consultation (VVC). Such requests must not involve new procedures, but may involve minor changes to already approved procedures, such as the frequency, duration or number of procedures performed; the type or dose of medication used; or the method of euthanasia. To request a VVC, the researchers should complete a consultation form and submit it to orsp@acu.edu. The request will be sent to the veterinarian who will determine if the requested change is permissible under VVC, conduct the consult, and either approve the request, recommend revisions or defer the decision to the IACUC.

h. Notify investigators and the institution in writing of its decision to approve or withhold approval of those activities related to the care and use of animals, or of modifications required to secure IACUC approval as set forth in the AWA/AWR policy. The IACUC procedures to notify investigators and the institution of its decisions regarding protocol review are as follows:

The chair communicates in writing the approval, request for clarification prior to approval, or request for specific changes to the investigator, who then submits a revised protocol, if necessary. The investigator must provide requested material in a timely matter before approval of the research protocol. The chair provides a letter indicating IACUC approval.

The Institutional Official is informed of IACUC actions through semi-annual reports, and as appropriate, written reports submitted by the IACUC chair at other times during the year.

i. Conduct continuing review of each previously approved, ongoing activity at appropriate intervals as determined by the IACUC, but not less than annually. The IACUC procedures for conducting continuing reviews are as follows:

Investigators are notified by the IACUC Chair approximately 6-8 weeks prior to continuing review deadline. Submitted applications are distributed to the IACUC members in the same manner as new applications. Review procedures are conducted in the same manner as described in III.D.6 above.

j. Be authorized to suspend an activity involving animals. The IACUC procedures for suspending an ongoing activity are as follows:

In the event of a serious breach of guidelines, a special meeting of the IACUC is called to review the incident and determine appropriate responses. The committee shall vote whether or not to suspend research activity; a quorum must be present for this vote to take place and suspension must be by majority vote of those in attendance. Should it be deemed necessary to suspend a research activity, the chair communicates in writing to the Institutional Official and the investigator, outlining the details of the breach of guidelines and recommending suspension of research activities until appropriate remediation is completed. The Institutional Official has responsibility to assure that the investigator abides by the IACUC decision. In addition, the IACUC may determine that a report must be sent to appropriate oversight officials. In such a case, the chair will draft a report to be sent by the Institutional Official to appropriate authorities.

k. Authorized to determine when a study is exempt from AWA/AWR based on definition provided in Part 1 of the regulations, including studies involving non-covered species or the use of agricultural animals for agricultural purposes. Generally, the IACUC chair will make this determination. Individual researchers should not make this determination without IACUC consultation and confirmation of exemption. Researchers are still expected to follow standard ethical guidelines for the care and use of animals, even when studies are exempt from AWA/AWR.

E. The risk-based occupational health and safety program (OHSP), for personnel working around or having frequent contact with animals, is developed in consultation with the university’s risk management officer. This individual is invited to meet with the IACUC annually to update the committee about new regulations or when changes in current facilities or training are under consideration. The OHSP is based on identification of known hazards and development of procedures to avoid them. Principal investigators have primary responsibility for overseeing the individuals working with and around animals. The attending veterinarian is responsible for determining whether the procedures undertaken for animal care are appropriate according to current practice. Finally, the IACUC has responsibility, through regular reviews/inspections, to assure that all components of the OHSP program are consistent with policy.

Known hazards for species frequently encountered by ACU personnel include:

1) bites or scratches from rodents and birds;
2) possible allergic reactions from exposure to animals;
3) exposure to zoonotic diseases;
4) injuries from handling equipment.

Workers must be instructed in issues of personal health and safety, including:

1) the use of personal protective equipment to reduce exposure to allergens;
2) proper handling of animals to prevent bites or other personal injuries;
3) appropriate vaccinations or other preventative measures for protecting against zoonotic disease;
4) and safe handling of equipment.

Personnel are provided with lab coats, gloves and face-masks as appropriate. Workers are instructed not to eat or drink around animals, apply cosmetics or other such activities. They are also required to wash their hands upon completion of work with animals.

Workers are also instructed that in the event of any injury, however minor, they must report the injury to their supervisor for follow-up. Because most workers are students, any injuries would be handled through the campus health center and related services. Faculty and other staff would be eligible for workman’s compensation coverage should an injury be work-related.

Workers who have concerns because of pregnancy, illnesses or immunocompromised status will be encouraged to consult with their personal physicians regarding any special actions that must be taken. Where appropriate, workers may be assigned other tasks without penalty.

F. The training or instruction available to IACUC members, scientists and other personnel involved in animal research or teaching is as follows: Researchers are required to complete Animal Research/Working with the IACUC modules through AALAS. IACUC members complete these modules, as well as the IACUC member modules. These modules meet the federal requirements for basic training in the humane care and use of animals in research and teaching, in research or testing methods that minimize the number of animals needed to obtain valid results and that minimize pain and distress.

IV. Institutional Program Evaluation

All of this institution’s programs for activities involving animals have been evaluated by the IACUC within the last six months and will be reevaluated by the IACUC at least once every six months, in accordance with AWA. Reports have been and will continue to be prepared in accordance with AWA policy. All IACUC semiannual reports will include a description of the nature and extent of this institution’s adherence to the regulations and documents outlined in IID. Any departures are identified specifically and reasons for each departure will be stated. Where program or facility deficiencies are noted, the report will contain a reasonable and specific plan and schedule for correcting each deficiency. Semiannual reports of the IACUC evaluation will be submitted to the Institutional Official. Semiannual reports of the IACUC evaluation will be maintained by this institution and made available to outside officials, as required and upon request.

V. Record-keeping

A. This Institution will maintain for at least three years:

a. A copy of this policy and any modifications made to it.

b. Minutes of IACUC meetings, including records of attendance, activities of the committee and committee deliberations.

c. Records of applications, proposals and proposed significant changes in the care and use of animals and whether IACUC approval was given or withheld.

d. Records of semiannual IACUC reports and recommendations (including minority views) as forwarded to the Institutional Official (vice-provost).

e. Documentation of any IACUC-approved exception to the regulations.

B. This institution will maintain records that relate directly to applications, proposals and proposed changes in ongoing activities reviewed and approved by the IACUC for the duration of the activity and for an additional three years after completion of the activity.

C. All records shall be accessible for inspection and copying by authorized representatives/officials, as required, at reasonable times and in a reasonable manner.

The IACUC documents have been revised as of January 2018 and can be
found in the ORSP Canvas classroom. You may enroll in the classroom by
clicking here.
  • Amendment Request Form, Animal
  • Animal Research Request, Observation
  • Animal Research Request, Wildlife
  • Animal Research Request, NonWildlife/Captive
  • Consultation Form, Animal
  • Continuing Review Form, Animal
  • Inactivation Request Form, Animal
  • Reporting Welfare Concern, Animal
  • Signature and Assurance Form, Animal
  • Unanticipated Event, Noncompliance Form, Animal