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Clinical laboratory

Safety lab

Nuvisan delivers fast turnaround times on safety data due to co-localisation of our clinical laboratory with our Clinical Pharmacology Unit (CPU), enhancing the speed of safety decision-making for participants throughout the course of the trials. This seamless integration is further strengthened by the direct connection of our laboratory information management system (LIMS) to the eSource data capturing system of our CPU via a validated HL-7 interface. Orders and results are exchanged digitally, which, together with barcoding of the samples, helps ensure maximum data integrity.
Tube of blood is placed in a centrifuge for plasma lifting

Biomarker analysis

Our clinical laboratory provides biomarker analysis using advanced, fully automated in vitro diagnostic (IVD) devices and CE-certified tests. We offer over 280 parameters across clinical chemistry, immunochemistry, hematology, urinalysis and coagulation analysis. All processes, from sample receipt and management to data export, are integrated within our LIMS, helping ensure high data integrity for every analysis.
A scientist testing blood samples for biomarkers in a modern lab 

Safety and biomarker analysis capabilities

Our clinical laboratory in Neu-Ulm is co-located with our CPU, where sample analysis for safety monitoring is conducted both during screening and throughout the course of the clinical trials, providing comprehensive analysis of various safety parameters, including hematology, clinical chemistry, coagulation profiles, urinalysis, drug-of-abuse screening and serological tests.  

The laboratory employs CE-certified and vendor-validated tests on IVD devices provided by leading industry manufacturers. Our team of experienced professionals helps ensure the highest standards of accuracy and reliability. Moreover, Nuvisan implements both internal and external quality control measures to maintain high quality and compliance with regulatory standards.

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