We’ll support your mammalian toxicology studies with TK data to correlate safety and drug blood concentration levels in animal models.
We support your early clinical single or multiple ascending dose through late stage studies with robust methods to establish optimal dosage and dose frequency.
Our team will partner with you to compare pharmaceutical alternatives to evaluate therapeutic equivalents.
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.
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.
You’ll get comprehensive statistical data analysis for TK report integration into regulatory submissions using WinNonLin® and SAS™.