From acute tolerability through multi-year and multi-generational safety assessments, we provide a consultative, responsive experience. You will receive timely and reliable reports that meet or exceed regulatory guidelines. For over 40 years, Inotiv’s experienced and proven safety assessment teams have backed thousands of successful IND and NDA/BLA submissions. In addition to routine protocols, our flexible, fast, and responsive team routinely develops custom protocols to meet our clients’ challenges. Our GLP toxicology services are comprehensive. Along with the in vivo conduct, we also provide:

  • Full histopathology support
  • Clinical pathology services
  • Dose formulation analytical development, validation, and analysis
  • Bioanalytical development, validation, and analysis
  • Pharmacokinetics/toxicokinetics (PK/TK) data analysis and interpretation

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