Our services include:

  • Pharmacokinetic-Pharmacodynamic (PK/PD) and toxicology study design assistance.
  • Drug concentration determination in various biological matrices (i.e. blood, urine, synovial fluid, cerebrospinal fluid, CSF) utilizing Liquid Chromatography-tandem Mass Spectrometry (LC-MS/MS) and Gas-Chromatography (GC-MS).
  • Development/validation of methods for approved and novel therapeutics according to the Food and Drug Administration’s (FDA) Compliance Guidelines for Analytical Method Validation.
  • Pharmacokinetic (PK) analysis

The average turnaround time for reporting of drug/toxicant concentration data is 4-6 weeks.  If method development and validation is required (novel drug or toxicant to the lab) discussion will determine the complexity of the project and estimated time for completion.

For PK data analysis the average turnaround is 3 to 4 weeks.

Have a project in mind? Submit an inquiry now!