In biopharmaceutical research, the potential for sample degradation exists at every level of the supply chain. Proper chain-of-custody documentation and good laboratory practice (GLP) standards can prevent corruption of samples, but biopharma labs may not have systems in place that allow for operational transparency among internal and external parties and suppliers.
Simplicis has years of experience developing customized sample management solutions for research laboratories. We conduct a thorough analysis of workflows, hardware, and software to identify opportunities for process improvement and sample control. We then integrate solutions, building APIs that unite disparate components and remove data silos.