A LIMS that helps my lab offer cutting-edge technologies to our patient population and meet regulatory requirements?
Laboratories that work with patient populations and introduce complex multi-step technologies must balance the demands of these highly regulated environments and still keep pace with the constant progression of technology.
These labs must maintain strict data collection standards, create detailed documentation of procedures, validate processes and institute enforcement of developed standard operating procedures (SOPs), all while ensuring their LIMS supports the latest technology. Clarity LIMS was built specifically for regulated laboratories so that they can bring the latest technologies, such as genomics and mass spectrometry, to their patient populations.
When evaluating a LIMS to support accreditation efforts, regulated organizations should find a system that:
- Ensures positive identification and sample integrity.
- Enforces laboratory SOPs for workflows and data collection.
- Collects data for the support of instrument and sample precision monitoring requirements.
Experience it in person – Request a demo
Learn from a customer – Read the EdgeBio case study
Read more about our support for clinical labs – Read the clinical brochure
See Clarity LIMS in action
From the EdgeBio Blog
“Given the level at which we want to be working, the LIMS not only lends credibility to our initiative as it’s reviewed by governing bodies, but also helps in preventing sample issues and ensuring we are doing what we say we are.”
– Justin Johnson, Director of Bioinformatics, EdgeBio
Conducting Clinical Next-generation Sequencing: How to Manage Change, CLIA, and Informatics
This white paper offers advice from two industry experts, Jill Northup from Medical College of Wisconsin, and Philip Cotter from ResearchDx, in the area of setting up a clinical NGS laboratory.
Clinical Features in Clarity LIMS: A Complete Solution for Regulated Laboratories
Clarity LIMS provides capabilities that help lab directors meet and demonstrate the following CLIA guidelines: Specimen identification and integrity, Procedure Manual, Control Procedures, Lab Director Responsibilities, Test records.
