LabConnect
has released its proprietary clinical trial sample tracking and management service, SampleGISTICS™.
Today’s clinical trials have increasingly complex analytical requirements that necessitate the utilization of multiple testing and biostorage facilities worldwide. This has led to gaps in sample visibility and downstream data management issues. “LabConnect developed this sample tracking service because of our clients’ need to locate their samples and data to effectively manage complex global clinical trials,” said Eric Hayashi, President and Chief Executive Officer. “Central laboratories have filled logistical and distribution gaps, but did not historically track the life cycle of samples, resulting in millions of dollars in unnecessary expenses, such as, lost samples, payroll costs, and time. LabConnect has the solution.”
The backbone of SampleGISTICS™ is LabConnect’s proprietary software, SampleREACH™, which provides Web-based, real-time sample tracking including collection, shipment, and receipt at any laboratory or location worldwide. In addition, the software enables instant accessioning, resulting in immediate identification and correction of queries including sample collection issues. SampleREACH™ provides detailed information about clients' samples including location, temperature, volume, freeze/thaw cycles, clinical data and has the ability to extract customizable reports. The tool’s forecast module makes budgeting more efficient and identifies when samples are missing.
As part of LabConnect’s complete laboratory services spanning a worldwide network of laboratories, SampleGISTICS™ eliminates the need to manually track samples by consolidating all of the information to one location. SampleGISTICS™ aims to significantly decreases the workload of site and clinical operations staff, allowing for faster decision making and a cost effective outcome.
Telemedicine Considerations When Conducting Decentralized Clinical Trials
January 14th 2025Compliance with state telemedicine requirements is imperative, as not only will most clinical trial sponsors contractually require such compliance, but non-compliance may also subject the practitioner to licensure violations and liability.
Driving Diversity with the Integrated Research Model
October 16th 2024Ashley Moultrie, CCRP, senior director, DEI & community engagement, Javara discusses current trends and challenges with achieving greater diversity in clinical trials, how integrated research organizations are bringing care directly to patients, and more.