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Inotiv’s team of experts provide the resources, instrumentation, and technology needed to help navigate your molecule through the various stages of the drug development process. We offer a full array of services and capabilities to efficiently move you to first-in-human and beyond.

To talk to an expert about our Bioanalytical Services, please click here.

Rapid Discovery LC-MS Bioanalysis

  • Nonclinical and Early Phase Preclinical Programs and Studies
  • Pharmacokinetic (PK) and Toxicokinetic (TK) Programs and Studies
  • In Vitro and In Vivo Sample Analysis
  • Stage-Appropriate Bioanalysis (Level 1 for screening; Level 2 for non-GLP IND-enabling)
  • Tissue Bioanalysis
  • Contemporary Bioanalytical Platforms and Technology

To learn more about our Nonregulated Discovery Bioanalytical services click here.

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Preclinical Through Clinical LC-MS Bioanalysis

FDA, EMA, and OEDC compliancy

  • Preclinical Programs and Studies
  • Pharmacokinetic (PK) and Toxicokinetic (TK) Programs and Studies
  • Clinical Study Support
  • In Vitro Bioequivalence Study Support
  • In Vitro and In Vivo Sample Analysis
  • Tissue Bioanalysis
  • Contemporary Bioanalytical Platforms and Technology
  • Method Transfer(s)
  • Method Development and Validation

To learn more about our Regulated Bioanalytical services click here.

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