We provide a full spectrum of toxicology advice, reporting, study review and project management.

Our experience spans from large pharmaceutical clients to virtual biotechs, from large-molecule to small-molecule projects, across a variety of therapeutic disease states. We actively participate in study design, compound screening and testing to help clients identify leading drug candidates.

• Direct preclinical toxicology studies for small molecules (new chemical entities) and large molecules (biotherapeutics—peptides, proteins, monoclonal antibodies, nucleotides).
• Provide strategic preclinical toxicology development plans, including strategies for determining mechanisms of toxicities and their potential relevance to humans.
• Prepare toxicology study budgets.
• Design studies using various routes of administration with both rodent and non-rodent species.
• Prepare and review protocols for all types of toxicology studies.
• Monitor toxicology studies and collaborate with CROs as well as research groups.
• Write toxicology reports within a quick timeframe.