Preclinical and Clinical Sample Analysis

A broad array of studies to meet your needs.

Nonclinical toxicokinetic (TK) studies

We’ll support your mammalian toxicology studies with TK data to correlate safety and drug blood concentration levels in animal models.

Clinical PK/Bioavailability studies

We support your early clinical single or multiple ascending dose through late stage studies with robust methods to establish optimal dosage and dose frequency.

Bioequivalency studies

Our team will partner with you to compare pharmaceutical alternatives to evaluate therapeutic equivalents.

Therapeutic drug monitoring studies

We provide an integrated service with our Central Laboratories to help you reduce errors, provide chain-of-custody sample tracking, coordinate sample shipments and integrate your reports for regulatory submissions.

Drug-drug interaction studies

We’ll help you with robust methods and rapid data turnaround time to assess the potential impact of drug-drug interactions. We publish all nonproprietary methods.

PK-TK analysis and reporting

You’ll get comprehensive statistical data analysis for TK report integration into regulatory submissions using WinNonLin® and SAS™.

Sample Analysis at Covance