STANDARD PROGRAMS FOR PHARMACEUTICALS, AG-PRODUCTS AND INDUSTRIAL CHEMICALS
IPMC-TMC in association with various GLP certified contract laboratories performs the complete standard programs as required by EPA, FDA, J-MHW, METI, EU and OECD for pharmaceuticals, AG-products and industrial chemicals (see Complete Packages).
- For Pharmaceuticals this includes nearly all pre-clinical safety assessments (Toxicology, Pharmaceutical Quality Control, Analytical Chemistry, Genotoxicity/Cytotoxicity, Pharmacology, Pharmacokinetics/ADME, Implant Studies, Animal Breeding, Regulatory Affairs and Consulting)
- For AG-Products this includes all the appropriate tests in compliance with current regulations (Toxicology, Analytical Chemistry/Residue Analysis, Physico/Chemical Properties, Kinetics/ADME, Ecotoxicology, Environmental Fate and Behavior, Regulatory Affairs and Consulting)
- For Industrial Chemicals this includes all necessary tests performed for Material Safety Data Sheets, Health and Environmental Risk Assessments, Notification of Chemicals (Base Set) for any country in the world in which the product should be marketed (Toxicology, Analytical Chemistry, Genotoxicity, Physico/Chemical Determinations, Ecotoxicology, Regulatory Affairs and Consulting).
One of IPMC-TMC’s strengths is their long experience in renal toxicology and carcinogenesis. Thus IPMC-TMC offers standard programs, tailored solutions, and investigative toxicology using in vivo and in vitro approaches in conjunction with collaborating GLP certified contract and academic research laboratories. IPMC-TMC also offers initial pathological assessment of kidney sections from an experienced toxicologist specialized in renal pathology (toxicology and carcinogenesis).