We provide comprehensive bioanalytical services compliance with regulatory requirement
Method development and validation
We provide need based validation protocols and parameters in accordance with US FDA guideline and also as per other guidance
- Small molecules
- Partial or full method development
- Estimate the plasma concentrations of test substances and pharmcokinetic parameters using validated software
- Estimate the concentrations of test substances in biological matrices including serum, synovial fluid, urine, cerebrospinal fluid and quantification of concentration in tissues
- Toxicokinetic studies
- Bioanalytical method development and validation as per the regulatory guidelines
- Bioanalysis with GLP compliance and estimation of toxicokinetic parameters using validated software