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Complete Your Scientific Evidence Package
Forge a path to market with nonclinical and toxicology research, where safety, efficacy, and regulatory compliance intertwine. As a trusted provider of comprehensive nonclinical and toxicology services, we enable our clients to navigate the complex landscape of product development with confidence.
Your Clinical Data Only Tells One Part of the StoryMany ingredient developers invest in efficacy studies but overlook the toxicology studies needed to create a comprehensive scientific evidence package. The result? Questions later in product development, regulatory review, or commercial partnerships. |
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Support Smarter Product Development
From research strategy to program oversight, build the safety data needed to move forward with confidence.
Plan
- Pre-screening
- Study strategy
- GLP-compliant study design
- Study planning (e.g. OECD)
Execute
- Study placement and monitoring
- Global laboratory coordination
- GLP-compliant oversight
Evaluate
- Genotoxicity
- Oral toxicity
- Reproductive & developmental toxicity
- Pharmacokinetics (PK)
- Proof of concept
- Mechanism of action
Not sure what your ingredient needs?
Whether you're starting with an idea, reviewing an existing data package, or preparing for commercialization, our scientists can help determine the most appropriate research program for your ingredient.
Connect With Our TeamModern Ingredients Require Modern Safety Science
Historical use doesn't always answer today's safety questions. Natural ingredients (including botanicals, probiotics, and other novel ingredients) often undergo processing, extraction, concentration, or formulation changes that may influence their safety profile.
A thoughtful safety study strategy helps support scientific confidence while reducing uncertainty during development.
Our team helps you identify what's missing and develop a strategy that supports your path to market.
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Equipped with a deep understanding of the unique challenges and regulatory requirements in this field, our qualified team of board certified toxicologists and scientists will guide and coordinate every phase of your project.  |
Supporting the Ingredients Driving Innovation
Our team of experts have experience across today's fastest-growing ingredient categories. Whether you're developing a novel ingredient or expanding an existing portfolio, we help build safety data packages for a wide range of product categories, including:
Flexible Options
We offer flexible options to cater to your specific needs in the nonclinical and toxicology service area. Choose from our diverse range of study models, including proof of concept, acute, 14-day and 90-day repeat dose studies as well as extended 2-year studies, ensuring comprehensive evaluation and enabling you to make informed decisions for your product or ingredient's safety and efficacy.
