 | The Clinical Protocol Manager module provides a template-driven interface that summarizes the clinical protocol objectives, describes the treatment group stratification, dosing, specimen collection and handling, the appropriate testing, and the visit/assessment schedule.
The clinical trial schedule tab defines the requirements of each timepoint by treatment group.
As the clinical trial progresses, LabWare LIMS enforces the rules and parameters defined within the approved protocol, including those regarding specimen collection, storage and handling, testing, identification and labeling, shipping, etc.
Protocols can be routed through a configurable multilevel approval process using the LabWare LIMS Approval Manager. |