Agilex Biolabs have 20 years’ experience in performing regulated bioanalysis, including quality method development, method validation and sample analysis services. We have successfully supported hundreds of preclinical and clinical trials around the world.
Our FDA-inspected Australian bioanalytical facilities have OECD GLP recognition with NATA and ISO 17025 Accreditation with NATA. Technical work is performed to meet FDA and EMA guidelines, providing our clients with a globally accepted basis for drug approval. Our client base includes leading pharmaceutical and biotech companies in Asia, Europe and the USA.
When you partner with Agilex Biolabs, you can be confident that your project will be delivered by the experts on time and with the highest quality results.