TetraQ is a NATA accredited, GLP recognised facility, with over 10 years in operation developing and validating bioanalytical methods to determine drug concentrations in a variety of matrices and conducting sample analysis in support of clinical and preclinical trials.

TetraQ has GLP recognition for the conduct of both in vitro and in vivo toxicology services and has experience in undertaking complete preclinical study packages for inclusion in investigational new drug applications (INDs).

TetraQ conducts in house pharmacokinetic analysis using validated WinNonLin software, with the design of these studies tailored to suit the stage of development you are at and include common PK parameters such as Cmax, Tmax, t1/2, AUC, AUCinf, Cl, λz, Vd, F.