MAKE AN IMPACT WITH YOUR RESEARCH
It’s vital that clinical labs deliver accurate results. The STARLIMS Clinical Research LIMS software makes sure your lab’s samples are collected, handled and processed accurately throughout the entire sample lifecycle. The STARLIMS solution grows as your lab’s needs evolve, providing unrivaled flexibility and support of user-configurable workflows for a wide range of research projects, clinical trials, and laboratory processes. Feel confident in your ability to meet changing investigator needs and increasingly stringent regulations, all while providing accurate clinical research results.
MANAGE COMPLEX CLINICAL TRIALS FROM THE START
The STARLIMS Trial Manager provides users with the capabilities to define and configure many factors of a study including:
- Study protocols
- Treatment groups
- Subject/sample metadata
- Master schedule, including visit schedules, visit-specific subject metadata, visit elements, tolerance limits and visit sequence information
- Consent information and verification, in accordance with Institutional Review Board (IRB) and regulatory requirements, as well as subject preferences
- Use of templates and wizards to establish study-based reference ranges, reflexes, triggers, and reporting requirements
TRACK AND HANDLE SAMPLES SEAMLESSLY
- Delineate, identify, and locate specimens within a container or in storage by using barcode scan fields and graphical tools
- Track specimen’s home location, due date for return, and responsible individuals
- Enable researchers to reserve specimens for a specified time interval
- Add new specimen metadata attributes to use during queries
- Identify and resolve discrepancies between specimen/subject attributes (arrival condition, container, transit time, etc.) and clinical study requirements
- Access a full specimen’s history from accessioning to final disposal