Pharmacokinetics and Pharmacology
TetraQ provides non-routine and routine analysis of samples collected in clinical trials and conducts in house pharmacokinetic analysis using validated WinNonLin software.
We are more than happy to accommodate your requirements for interim pK reporting over the duration of your study, and can provide fast turnaround to meet ethics committee and dose review dates to ensure the smooth running of your clinical trial.
The design of these studies are tailored to suit the stage of development and include common PK parameters (e.g., Cmax, Tmax, t1/2, AUC, AUCinf, Cl, λz, Vd, F) as well as descriptive statistics (count, mean, standard deviation, standard error, % coefficient of variation (CV), minimum, median, maximum, geometric mean, and % CV of the geometric mean) which are also reported for each of the pharmacokinetic parameters.
TetraQ also has the capabilities to conduct bio distribution studies on request.