Preclinical Study Coordination and Management

ToxiSan's expertise in toxicological and ecotoxicological fields and selected partners with testing facilities can deliver experimental services together with regulatory compliance/notification in one package.  ToxiSan's experienced scientific staff has conducted thousands of toxicity studies for the pharmaceutical, biotechnology, chemical, food and consumer products industries:

ToxiSan provides a non-clinical research and development program designed with the clinical trial as the goal and offers:

• Coordination of laboratory evaluation and selection
• Good Laboratory Practice (GLP) compliance
• Study costing
• Protocol development
• Study monitoring
• Auditing

ToxiSan supports the following study types:

• GLP compliant
• EPA, FDA, OECD, ICH, MAFF, EU, ISHL and MOHW
• Complete range of studies
• Acute (including eye and skin irritation and sensitization)
• Experienced with all standard laboratory animal species
• Routine and specialized routes of administration to include: oral, inhalation, intravenous injection, infusion, percutaneous, dermal, ocular, vaginal, rectal, urinary bladder catheterization, customized routes of administration (interventricular).

Phone: (877) 421-0316