TOX-RSA provides consulting services in toxicology, pharmacology, biocompatibility, and other regulatory-driven nonclinical sciences related to medical products.   Our practice areas include small molecule pharmaceuticals, biologic therapeutics (including biologic oncology drug products), medical devices, and combination products.   We develop, implement, and manage strategic nonclinical testing programs (from early stage preclinical discovery, through clinical development, and post-approval), interpret and critically analyze nonclinical data, perform data gap analysis, identify vulnerabilities, and trouble shoot throughout a product’s life cycle.   We are committed to providing objective, scientifically sound, effective, and practical solutions and to developing strong, synergistic relationships with our clients.