Arivita, LLC

With extensive physiology, pharmacology, and toxicology experience in in vitro and in vivo studies, as well as experience on both the client and CRO sides of projects, we have unique insight to help meet the needs of your internal and external stakeholders. We assist in all facets of the project lifecycle from study design through reporting, regulatory filings, and/or publication. Consulting services available include: • Study design • CRO project management and monitoring • Data review, interpretation, and reporting • Toxicological evaluation of ingredients • Hazard screening • Scientific writing and editing • Literature reviews • Risk assessment and toxicological evaluation program development • Engagement strategy development for novel products • Improvements in laboratory efficiency, in vitro toxicology methods, and regulatory guideline compliance • Custom projects to meet individual clients' needs