Quality assured preclinical & clinical testing solutions


TetraQ is a NATA and ISO 17025 accredited, GLP recognised facility, with over 10 years 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).

Pharmacokinetics & Pharmacology

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.

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Technical infrastructure

Information about the laboratories and technical infrastructure More...


TetraQ has experience in supporting clients to meet the REACH requirements More...

Quality System

TetraQ operates within a quality framework in compliance with international standards More...

Fact Sheets

TetraQ Capabilities

Overview of Capabilities and Services


ADME-Bioanalytical Capabilities


TetraQ - Birds Eye View

A one-page overview of TetraQs services and capabilities

All Factsheets