Clinical Trial Sample & Consent Tracking
Follow the patient, follow the sample. Patient samples are the lifeblood of your biomarker-driven clinical trials. Our unique software solution tracks these samples through their lifecycle across the ecosystem of sites, labs, biorepositories, and other trial partners.
Your study teams are empowered with up-to-date, accurate and actionable insights on biospecimen and related patient informed consent activities, boosting trial execution productivity while reducing operational and compliance risks for both ongoing trials and future translational medicine studies.
Next Generation Biobanking
A biobank is a liability, not an asset – unless and until it can provide significant value for scientific research. LIMS traditionally treats biobanking as a stand-alone activity, but we see the biobank as just one component in an integrated translational and clinical research ecosystem.
This requires an IT solution that seamlessly supports data integration, data management, and advanced search capabilities, in addition to operational biobanking workflows. With Next Generation Biobanking, you can reap the benefits of a well-annotated patient and sample database that supports precision medicine, clinical trials, translational research, and patient registries.
Data Exploration, Supercharged
Navigating the path to precision medicine is quickly becoming a "big data" problem, necessitating the harmonization of disparate healthcare, biomarker, clinical research, and real world evidence data sets.
The ability to integrate, standardize, and turn the various sets of “big data” into “smart data” is key to producing scientific insights. Our patented Qiagram technology empowers scientific minds in hypothesis generation and evaluation by allowing researchers to easily ask sophisticated ad hoc questions about complex data sets via an intuitive visual interface.
Outsourced Biospecimen Management Services
Supplement your biospecimen management team with our employees, or outsource the entire biospecimen lifecyle management process to us. In conjunction with Labmatrix™ and Qiagram, the world class biospecmen and consent lifecycle management tools from BioFortis
, we can manage issue identification and resolution, root cause analyses, and continuous improvement on your behalf.
Consent Codification & Management Services
The implementation of electronic consent in clinical trials continues to evolve. Our consent codification and management services provide the resources and capabilities to digitize and codify consent parameters, so that patient consent can be associated with samples, to assist sponsors in finding and utilizing samples for future use.
“After putting Labmatrix in service, we gained new abilities to review and analyze sample data, including trends by site, country or vendor, a full chain of custody across our vendors, and sample expiry and other consent-driven activities.” — Director, Clinical Operations