Contract Testing Expertise Across Regulated Industries
From cosmetic safety assessments to pharmaceutical toxicology and veterinary product development, our integrated testing platform serves the diverse needs of life sciences companies worldwide. Every study is designed to meet the specific regulatory requirements of your target market.
Cosmetics Companies
We partner with global brands, independent labels, and contract manufacturers to generate the safety data required for market authorization across FDA, EU, and international jurisdictions. Our integrated study designs address multiple regulatory frameworks in a single testing program, reducing both cost and time-to-market for multi-market launches.
- Dermal irritation & safety (OECD TG 404)
- Ocular irritation testing (OECD TG 405)
- Skin sensitization assessment (OECD TG 429)
- Photoirritation & phototoxicity
- Product stability testing
Human Pharmaceutical Producers
Our preclinical toxicology program supports pharmaceutical companies from early-stage dose-ranging through the comprehensive chronic studies required for IND applications and NDA submissions. We have experience across oncology, CNS, cardiovascular, metabolic, and anti-infective therapeutic areas, with study designs that satisfy FDA, EMA, and ICH requirements.
- Preclinical toxicology (acute, subchronic, chronic)
- Dose-range finding & MTD studies
- Reproductive & developmental toxicity (ICH S5)
- Carcinogenicity bioassays (ICH S1)
- Safety pharmacology core battery (ICH S7)
Veterinary & Animal Health Companies
We support veterinary pharmaceutical and biological product developers through every stage of the regulatory pathway. Our facility maintains purpose-bred colonies of the target species required for FDA-CVM and USDA-CVB submissions, with BSL-2 containment for controlled challenge studies and field simulation capabilities.
- Target animal safety (TAS) studies
- Vaccine efficacy & immunogenicity trials
- Palatability & preference testing
- Field safety & effectiveness studies
- Biological product testing (9 CFR 113)
Agrochemical / Pesticide Producers
Our environmental and agricultural toxicology program generates the safety and residue data required for EPA FIFRA registration and EFSA authorization. We support crop protection, feed additive, and growth promotant companies with study designs that address both domestic and international regulatory requirements.
- Environmental toxicology assessments
- Target species safety evaluations
- Residue chemistry & depletion studies
- Ecological risk assessment support
- EPA FIFRA & EFSA registration studies
Medical Device Manufacturers
Our ISO 10993 biocompatibility testing program provides the complete biological evaluation required for FDA 510(k) clearance and PMA approval. We execute the full test battery from a single facility, ensuring consistency across all endpoints and streamlining the regulatory submission process for device manufacturers.
- ISO 10993-5 Cytotoxicity
- ISO 10993-10 Sensitization & irritation
- ISO 10993-6 Implantation studies
- ISO 10993-11 Systemic toxicity
- ISO 10993-3 Genotoxicity battery