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.
- 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.
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.
In Vivo Services
Pathology
Surgical Models and Medical Device Testing
Drug Metabolism and Pharmacokinetics (DMPK)
Consulting