The solution to high-risk regulatory toxicology problems
Providing cientifically rigorous, defensible assessments for complex ingredients, impurities, and regulatory decision-making.
Providing cientifically rigorous, defensible assessments for complex ingredients, impurities, and regulatory decision-making.
At ToxVeritas, we specialize in translating complex toxicological data into clear, defensible safety conclusions.
With expertise spanning regulatory frameworks and product safety, we support organizations in making informed, compliant, and strategic decisions.
Our approach integrates scientific depth, regulatory precision, and emerging intelligent systems to deliver high-quality, reliable outcomes.
PhD-level toxicology expertise with a strong foundation in mechanistic and regulatory science.
Aligned with global safety frameworks to ensure defensible and compliant outcomes.
Integrating data-driven methodologies and advancing toward AI-enabled toxicology solutions.
Comprehensive safety evaluation of impurities and degradants, including genotoxicity assessment, threshold justification, and margin of exposure analysis.
Assessment of active ingredients, excipients, botanicals, and formulations for safe use in pharmaceutical and consumer health products.
Preparation of regulatory-ready documents, including CTD-style toxicology sections, safety narratives, and risk assessments.
Strategic guidance aligned with global regulatory frameworks including FDA, EMA, EFSA, and ICH to support product development and compliance.
Comprehensive review of available data, including hazard identification and mechanistic evaluation.
Exposure assessment, dose-response evaluation, and risk characterization using established toxicological principles.
Clear, actionable recommendations aligned with regulatory expectations and business objectives.