TRUSTED CONTRACT TESTING PARTNER

Rigorous Science.
Reliable Results.
Regulatory Confidence.

For over 25 years, Meramec Bio Eval Center has delivered GLP-compliant safety and efficacy testing to pharmaceutical, veterinary, and cosmetic companies worldwide. From preclinical toxicology to regulatory submission support — one laboratory, complete confidence.

25+ Years of Excellence
5 Species Tested
200+ Global Clients Served
10,000+ Tests Completed

Regulatory Compliance & Accreditations

GLP Certified

Good Laboratory Practice — FDA 21 CFR Part 58 & OECD Principles

USDA Registered

Animal Welfare Act compliance with IACUC oversight

FDA Compliant

CDER, CBER, CVM & CDRH submission support

OECD Guidelines

Internationally accepted test guidelines for mutual data acceptance

EPA FIFRA

Agrochemical & pesticide safety evaluation compliance

ICH Harmonized

Global pharmaceutical development standards S1–S11

What We Do

Comprehensive Contract Testing Services

From early-stage toxicology through regulatory submission, our integrated service platform supports the full product development lifecycle.

Animal testing laboratory
Core Capability

Animal Testing Services

GLP-compliant studies across dogs, cats, rodents, poultry, and livestock. Purpose-bred colonies with full veterinary oversight and USDA-registered facilities.

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Pharmaceutical research laboratory
Human Health

Pharmaceutical Testing

Preclinical toxicology, dose-ranging, ADME, and pharmacokinetics studies supporting IND applications and regulatory submissions worldwide.

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Cosmetic safety testing
Consumer Products

Cosmetic Safety Testing

Dermal irritation, sensitization, ocular safety, and stability testing per OECD guidelines. Data packages accepted by FDA, EMA, and PMDA.

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Veterinary research studies
Animal Health

Veterinary Studies

Target animal safety, palatability, vaccine efficacy, and field trial support for veterinary pharmaceutical and biological product development.

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Laboratory safety and efficacy testing
Study Design

Safety & Efficacy Studies

Acute, subchronic, and chronic toxicology. Reproductive and developmental toxicity. Carcinogenicity assessments per ICH and OECD guidelines.

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Regulatory affairs team
Regulatory Affairs

Regulatory Support

GLP documentation, regulatory strategy consulting, and submission-ready data packages for FDA, USDA, EMA, EPA, and international authorities.

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Industries We Serve

Trusted Across Regulated Industries

We partner with R&D teams, regulatory affairs professionals, and procurement managers across the life sciences sector.

Cosmetics and personal care products

Cosmetics & Personal Care

Dermal safety, sensitization, and ocular testing for skincare, haircare, and cosmetic formulations. Integrated study designs accepted by FDA, EU, and PMDA for multi-market submissions.

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Pharmaceutical industry

Human Pharmaceuticals

Preclinical toxicology, pharmacokinetics, and safety pharmacology studies supporting IND/NDA applications. Experience across oncology, CNS, cardiovascular, and metabolic therapeutic areas.

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Veterinary and animal health

Veterinary & Animal Health

Target animal safety, vaccine efficacy, palatability studies, and field trial support for companion animal and livestock product development. USDA-CVB and FDA-CVM expertise.

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Ready to Advance Your Product Development?

Our scientific team will design a GLP-compliant study protocol tailored to your compound, timeline, and target regulatory markets. Contact us to discuss your project requirements.