LIMS for Clinical Research
No matter what type of research lab you work in, you know first-hand just how demanding laboratory research can be. From testing and storing specimens to documenting results and preparing for regulatory audits, the operational challenges you face can be tremendous. And the use of manual processes or outdated information management systems only adds to these challenges, leading to a loss of productivity and a greater potential for errors.
That's why we developed the STARLIMS Clinical Solution.
A comprehensive solution designed to streamline and automate the specimen lifecycle process, STARLIMS greatly mitigates your most labor-intensive processes. Not only is it a fully scalable solution with the ability to grow as your needs evolve, it also offers unrivaled flexibility and supports user-configurable workflows for a wide range of laboratory processes. Above all, you can feel confident in your ability to meet changing investigator needs, comply with increasingly stringent regulations and produce the highest-quality results through our automated lab processes.
Learn more by viewing our Clinical LIMS Brochure.
LIMS for Biorepositories
As a researcher involved with managing a biorepository it's not only imperative that you maintain sample integrity and produce high quality data, but that you're also able to market the data you capture and meet increasingly stringent regulatory requirements. Efficiency is paramount to time and cost savings, but it must never come at the expense of quality. Your customers depend on your ability to manage and distribute high-quality specimens, and the failure to do so can have a direct impact on your business.
STARLIMS is a comprehensive solution designed to increase operational efficiency while improving the quality of your specimens and sample data by offering the following.
Ready-made workflow, shipping and interoperability tools meet a wide range of lab processes from managing plate-based DNA/RNA extraction to automated specimen handling systems to complete ordering, packing and shipping solutions.
Track chain of custody with electronic signatures to ensure that the full genealogy and history of the specimens are maintained while enforcing the appropriate business logic for approval of specimen usage or movement.
Reliably manage large volumes of samples and easily modify workflows to accommodate your organization's growth and evolving needs.
Learn more by viewing our Rutgers case study and Biorepository brochure.
LIMS for Clinical Trials
As a lab researcher or manager involved with clinical trials you understand the need to get it right the first time. Not only are you responsible for performing tests and monitoring data but you must also manage specimens and track shipments. Chances are you're using separate software systems to perform each of these functions. This lack of software integration not only magnifies an already complex process, causing a significant loss of productivity, but it can also greatly hinder the quality of your research.
Study sample management
The STARLIMS Clinical Solution provides powerful tools to manage clinical study specimens and all aspects of testing, storage, distribution and reporting.
Identification of high-value biomarker specimens
Enhanced functionality allows for rule-based screening of incoming clinical trial specimens to ensure proper storage and handling and to identify high-value biomarker specimens and alert investigator site personnel to capture the specimen and any important ancillary data, obtain patient consent and provide instruction on appropriate handling and shipment procedures.
Direct global access
Powerful features provide secure and direct global access to central laboratory operations for key stakeholders including lab personnel, clinical trial investigators, project managers, kit manufacturing sites and external reference labs.
Advanced tools streamline the setup process by enabling the use of existing studies as templates for new studies and configuring wizards to facilitate study-based reference ranges, reflexes, triggers and reporting requirements.
Learn more by viewing our case studies and articles: