Clinical Trials LIMS
A Configurable Clinical Trial LIMS for Your Laboratories
Unlike most healthcare laboratories, there is nothing routine about clinical trial labs. No two trials are alike. Each one has a unique combination of protocols, assays, specimen types, patients, employees and more. Your lab must manage this complexity while complying with an extra layer of regulation and oversight. LabLynx’s ELab LIMS for Clinical Trial Laboratories delivers the easy configurability, security and scalability you are looking for.
You can configure ELab LIMS to manage and report every aspect of a clinical trial. Simple administrator interfaces let your lab’s staff quickly set up the protocols, specimen types, and other elements of the trial while streamlining workflows. From encrypted cloud storage to strictly limited user access permissions, ELab LIMS protects proprietary data and patient information. Also, automated report generation simplifies reporting to institutional review boards, NHS HSS and the Clinical Trial Database.
Designed for the Unique Nature of Clinical Trials
Configure for Each Trial
ELab LIMS has the flexibility and feature depth needed to conform with your lab’s trials and workflows, getting out of the way so you can produce results.
Sample Tracking and Batching
ELab LIMS provides full chain-of-custody tracking by sample — or by sample group — to reduce pre-analytical errors and make audits more efficient.
Secure Cloud Database
Provide your investigators convenient anywhere, anytime access to trial data without compromising the integrity of your trials or the confidentiality of patient information.
Integration and Automation
Your trials become more productive when you eliminate manual processes by integrating your lab’s instruments with ELab LIMS and automating workflows.
Task and Event Scheduling
Schedule routine events such as a subject’s dosage administration with notifications to trial staff. Improve lab management by scheduling calibration, inspection and other events.
Electronic Laboratory Notebooks
Our ELN, ELab Notes, is scalable, auditable and secure. Integrate data with the images, forms and other documentation that each trial generates.
Reporting and Compliance
Automated reporting reduces the overhead of submissions to the Clinical Trial Database and IRBs while maintaining CLIA and other accreditations.
Training and Certifications
Manage and document training to keep your clinical investigators and staff certified on the latest standards and guidance in Good Clinical Practice.