MediaLab Document Control
MediaLab’s Document Control is a powerful way to manage your laboratory’s policies, procedures, and documentation. Our twenty years of expertise in clinical laboratories have created a document control solution that guides you to full compliance with all laboratory standards, regulations, and best practices. Document Control provides an automated, centralized platform for all of your document approvals, workflows, edits, sign-offs, audits, and more—with flexibility and customization features to match your laboratory’s unique needs.
MediaLab's Document Control supports:
• Digital records and version control of all documents,
• Standardization across all documents from all sites,
• Electronic signatures that meet 21 CFR Part 11 standards,
• Customized approval workflows and processes,
• Robust searching to easily locate specific documents, and more!
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Avalon Laboratory System
Sophisticated and HIPAA-compliant, the Avalon Laboratory System is specifically designed to manage the production and billing needs of clinical, esoteric, and toxicology laboratories. Developed by Computer Service & Support(CSS), this modular laboratory information system offers an array of features for reference laboratory automation. The solution also provides a rich set of modules for microbiology, pain management and toxicology, rescheduling, remote laboratory, SQL Access, electronic medical records, pharmacogenomics, and more.
In addition, there is Avalon BI (Business Intelligence) for billing. With Avalon LIS and Avalon BI running on the same platform, there is a reduction in errors and duplicate entry of data. The billing portion also offers up-front eligibility and diagnosis validity checking. In Avalon BI, there are even more robust reports for revenue cycle management.
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LabTrak
JRB Medical Associates, Inc. offers a unique laboratory information system that has helped countless medical professionals streamline the management of important patient diagnostics information and data. We have spent over 25 years in business focusing on the needs of the average physician office, as well as pain management clinics and specialty labs. Designed specifically for in-house laboratories, it is compliant with CLIA, HIPAA, and all other regulations regarding patient records. Our lab information system is essentially unique software that works with as many laboratory analyzers you are running. This allows any medical office to track and manage diagnostic results with ease. Whether you prefer manual management, or electronic record systems, this LIS is guaranteed to surpass expectations. The following are the different components that can be comprehensively handled within our single system.
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Qualis LIMS
Qualis LIMS is an enterprise-class laboratory information management system used in industrial, analytical, & commercial sample testing across several industry verticals such as pharmaceutical, life-sciences, contract research, clinical research etc.
Qualis LIMS has built-in integrated modules to manage all laboratory processes & help labs perform their tasks in an automated and paperless manner while enabling them to fulfil regulatory compliance requirements & adhere to industry standards.
It digitally transforms labs by helping them:
• In managing, storing, & aliquoting of samples.
• Record final results of tests & experiments - manage tests, projects, samples, instruments & inventory in one central secure database.
• Meet data integrity & regulatory compliance requirements such as GxP, ISO17025, 21 CFR Part 11 & EudraLex Annex 11 without any compromises.
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