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Species
Macaca fascicularis
The primary species for regulated safety evaluation, supported by GLP and non-GLP toxicology, safety pharmacology, PK/PD, and immunology under AAALAC-accredited, USDA-licensed standards.
Research applications
Repeat-dose and dose-range-finding toxicology with GLP-aligned documentation.
Cardiovascular, respiratory, and CNS safety pharmacology support.
Pharmacokinetics and pharmacodynamics for small molecules and biologics.
Antibody pharmacokinetics and immunogenicity testing for biologics.
Immunotoxicology and cytokine profiling in a regulated setting.
Study designs aligned to U.S. and international regulatory expectations.
The most widely used NHP in regulated safety evaluation, with extensive ICH and FDA precedent.
Scale from early investigation to submission-supporting studies within one facility.
Qualified supply and in-life execution together reduce handoffs and protect data traceability.
Resident veterinary professionals provide oversight and welfare assurance throughout conduct.
Quality & welfare
Exceptional care is the foundation of reliable data.
Yes. GLP and non-GLP study designs are available. GLP applicability depends on protocol, objectives, timeline, and facility fit. Protocol submission is the first step in confirming GLP suitability.