Replacement
Use non-animal methods, simulations, existing data, tissue systems, or other validated alternatives when suitable.
The JR Institute intends to permit animal research only through appropriate scientific justification, independent review, veterinary oversight, humane care, trained personnel, and ongoing monitoring.
This page presents a planned public standard. A qualified animal-care and use review process, veterinary program, facilities, training, and incident-reporting system should be established before animal research begins.
Animal research may be considered only when the question cannot be answered adequately through validated alternatives and when expected knowledge or public benefit justifies the work.
The Institute should apply replacement, reduction, and refinement throughout planning, approval, care, procedures, monitoring, and study completion.
Use non-animal methods, simulations, existing data, tissue systems, or other validated alternatives when suitable.
Use the minimum number of animals consistent with valid design, safety, and meaningful results.
Modify procedures, handling, housing, anesthesia, analgesia, and endpoints to reduce pain and distress.
Provide qualified veterinary authority over health, welfare, treatment, emergency care, and humane endpoints.
Require protocol review by qualified persons with scientific, veterinary, welfare, and community perspectives.
Permit procedures only by trained people working within approved qualifications and supervision.
This policy is intended to apply to live vertebrate animals used in research, testing, teaching, demonstration, breeding, field study, observation, or the development of biological materials.
Work performed through collaborators, contractors, field sites, or outside institutions should also meet applicable review and welfare requirements.
No covered animal activity should begin before a qualified review body has approved the scientific purpose, species, numbers, procedures, pain category, housing, endpoints, personnel, and veterinary plan.
Reviewers should be free of unmanaged conflicts and should have authority to require changes, suspend work, or withhold approval.
Investigators should explain why animal use is necessary and describe the search for suitable alternatives.
Convenience, habit, or historical practice alone is not sufficient justification for animal use.
Proposed numbers should be supported by scientific design, prior evidence, statistical reasoning, expected variability, breeding needs, attrition, humane endpoints, and avoidance of unnecessary duplication.
Too few animals may waste lives through an inconclusive study; too many may create unjustified harm.
Procedures should use appropriate anesthesia, analgesia, sedation, monitoring, supportive care, and humane endpoints unless a scientifically necessary exception receives specific justification and approval.
Unexpected pain or distress should trigger veterinary evaluation, treatment, protocol review, modification, or humane euthanasia when necessary.
Animals should receive species-appropriate housing, nutrition, water, sanitation, temperature, ventilation, light cycles, social conditions, enrichment, observation, and emergency care.
Exceptions should be scientifically justified, time-limited, independently reviewed, and monitored for welfare impact.
Personnel should be trained in species-specific handling, procedures, anesthesia, analgesia, aseptic technique, recognition of pain, emergency response, euthanasia, and recordkeeping.
Occupational-health programs should address allergies, bites, zoonotic disease, injuries, chemicals, biological hazards, reproductive risks, and other exposure concerns.
Material changes to species, numbers, procedures, pain level, personnel, housing, endpoints, drugs, surgery, or study purpose should be reviewed before implementation.
Immediate changes may be made when necessary to protect animal welfare, with prompt reporting afterward.
Unexpected deaths, injuries, escapes, prolonged distress, equipment failures, environmental problems, protocol deviations, inadequate care, or other welfare concerns should be reported promptly.
Good-faith reports should be protected from retaliation and reviewed by qualified, unconflicted personnel.
At study completion, investigators should reconcile animals, document outcomes, preserve required records, resolve unused specimens or materials, and arrange lawful, humane disposition.
Records should support traceability, welfare review, scientific integrity, sponsor requirements, and institutional accountability.
Framework date: July 2026
Inquiries may concern a proposed study, animal welfare, unexpected injury, inadequate care, environmental conditions, protocol deviation, or suspected noncompliance.
Identify the activity, location, species, date, concern, immediate risk, and any supporting information.
Contact the Institute