Our Sites
At Nexelis, a Q² Solutions Company, we built a state-of-the-art CRO, driven by scientific discipline, and aided by our advanced facilities and cutting-edge technology through our global network of specialty laboratories. Across the U.S. and Canada, Nexelis emerged from legacy companies Pacific Biomarkers, NEOMED-LABS, and PAIRimmune. With a combined 30 years of industry expertise, we were well-positioned to become the leading specialty lab for what’s next in therapeutic testing and development.
Since debuting the newly combined Nexelis brand in 2018, we have continued to add to our portfolio of services, bench of scientific experts, and global laboratory footprint with the acquisitions of ImmunXperts, AIT Bioscience, and GSK Vaccines Clinical Bioanalytical Laboratory in Marburg, Germany. We’ve also formed a strategic partnership with UK Health Security Agency ensuring that we deliver the diverse testing needed to our global sponsors.
Nexelis’ global network of laboratories serves as an extension of your own scientific teams to scale, quickly and efficiently to meet demands for specialty testing for all phases of development.
Laval, Quebec, Canada
Located just outside of Montreal, the Nexelis flagship is set in a dynamic cultural environment. It’s also part of a robust biopharma community.
Indianapolis, Indiana
Family-friendly “Indy” is home to the Indianapolis Colts and Pacers and the Indianapolis Motor Speedway. It’s also known as the heart of the “Biotech Midwest,” a nine-state region that contains more than 16,800 biotech companies.
Gosselies, Belgium
In the town of Charleroi, Nexelis’ Gosselies location is based in the Brussels South Charleloi Biopark, which provides a unique life sciences ecosystem. The area offers a brilliant scientific community, a high-quality clinical trial network, and a connection to Europe’s top financial center.
Marburg, Germany
Located north of Frankfurt, Marburg has the energy of a university town along with river views, a busy city center, and the historic Landgrave Castle. It’s also home to many pharmaceutical and biotech companies and CDMOs.
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State-of-the-Art Facilities
Our state-of-the-art facility design promotes scientific excellence through our team of scientists, highly automated workflows, and data management through Laboratory Information Management System (LIMS) systems — including our fully paperless electronic lab notebook (ELN) system used at our Indianapolis bioanalytical laboratory — to support client studies whether they are research based or require fully validated systems as per required standards, including 21 CFR Part 11 compliance. Documentation is preserved in internal and external archives with restricted access to safeguard data and study materials throughout the retention period.
Quality Management System
Our well-defined quality management system (QMS), seamlessly aligns with regulatory requirements and CLIA, GCLP, GCP, and GLP standards ensure compliance for our clients and for the studies we support.
Current Accreditations/Certifications
- NYSDOH — New York State (Biomarkers)
- GCLP (Bioanalytical, vaccines)
- GCP/GLP (Indianapolis)
- GLP (Beijing)
- AAALAC — Association for Assessment and Accreditation of Laboratory Animal Care (Preclinical Laval and Beijing)
- CCAC — Canadian Council on Animal Care (Preclinical)
- OLAW — Office of Laboratory Animal Welfare (Preclinical)
- BBL — Belgian Banking License (Gosselies)
Robust Data and Scientific Processes
We support your preclinical and clinical molecule/vaccine candidate development — with data and study sample testing managed by our validated, customized, LIMS and its full audit trail.
Sample Management
Our team provides the same uncompromising attention to detail whether you have 10 samples or a million. Each analytical and data plan is custom crafted to ensure we meet all deliverables for all stakeholders. Customized reporting delivers the specific data results you want, on the schedule you require.
Integrated Approach
Nexelis’ global scale and high-volume capabilities combines our high-touch, individualized service with the capacity and global coverage to move even the largest projects forward on time and on budget. All while adhering to regulatory requirements including chain of custody, IATA (International Air Transport Association) shipping guidelines, and sample verification upon receipt. We also provide both long- and short-term sample storage. Our fully integrated approach streamlines the management and handling of your data throughout the sample life cycle, resulting in accurate, actionable, and timely evidence.
