Charles River offers overall developmental and reproductive toxicology (DART) program planning and individual study design to conduct safety assessments for your products according to internationally recognized guidelines, including ICH and OECD.
We conduct male and female fertility, developmental toxicity (embryo-fetal development), pre- and postnatal development and multigenerational studies to assess the potential effects of pharmaceuticals, biopharmaceuticals and/or chemicals on the entire reproduction spectrum. A full range of rodent and nonrodent species are tested with dose routes ranging from dermal to intravenous infusion. A range of specialized functional evaluations is also available, including neurobehavioral testing and immunologic assays.
For additional information on our DART capabilities, including Researcher newsletters, webinars and historical control data, visit the Source℠.