Symbiont Research supports nonclinical contract research organisations, pharmaceutical and agrochemical companies, in the area of toxicology and risk assessment for product safety. We share the same level of involvement and commitment as our clients’ for the efficient preclinical development and are dedicated to assure scientific, regulatory, and data integrity. Available services, assist clients to overcome hurdles in design of tailored nonclinical programs (scientific & pragmatic/innovative regulatory strategies, cost effective/ optimized CRO interaction; insight in regulatory expectations & ensure regulatory compliance), interpretation of toxicological issues, preparation of regulatory dossiers, regulatory scientific advice procedures, direct management and monitoring of toxicology studies, assessment on critical safety issues of the drug products and gives insight in opportunities to lower costs and enhance speed and efficiency to next development stage/partnering opportunity. Symbiont Research also offers safety evaluation and monitoring of toxicological studies on veterinary medicines, medical devices and food additives in accordance with their respective regulations.