At Ardena we offer GLP compliant, pre-clinical bioanalysis services to support your in-vivo drug safety packages. We have extensive experience in developing robust bioanalytical assays in blood, plasma, urine and many other matrices such as tissues. Our pre-clinical assay validations are conducted in accordance with current regulations. When your compound is moving towards pre-clinical development and you need robust and validated assays to claim Good Laboratory Practice (GLP) for the pre-clinical safety studies, you are in the right place at Ardena.
We offer a fully GLP compliant pre-clinical bioanalysis service to support your drug molecule as it enters the pre-clinical development phase. Your samples will be stored in our secure monitored storage facility (-20°C or -80°C) until analysis.
By ensuring a fast turnaround of your sample analysis we can help with critical decision steps in your preclinical drug development process. Ardena’s customer portfolio consists of pharmaceutical companies and veterinary pharmaceutical companies.