- Download a White Paper
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LIMS - Total Cost of Ownership
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DataBanking
- Download a Data Sheet
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LIMS & Protocol Tracking
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LIMS & ABI Mass Spectometry
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LIMS & Affymetrix
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LIMS & Agilent
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LIMS & Illumina
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LIMS & Lab Automation
- In the News
- Dr. Claire Frazer’s lab at the Institute for Genome Sciences at UMAB Medical Center has licensed Exemplar LIMS Read Article.
- ExonHit Selects Exemplar LIMS. Read Article
- Childrens Hospital of Pennsylvania Selects Exemplar LIMS. Read Article
- Sapio Sciences Announces Exemplar LIMS Version 2 Read Article
Exemplar LIMS is redefining LIMS to address the complete pipeline from receipt of samples in the lab through clinical trial management. Designed in collaboration with some of the top pharmaceutical and research directors in the world, Exemplar LIMS combines unprecedented ease-of-use, breadth of functionality and customizability into one integrated product.
| Exemplar LIMS | Traditional LIMS | |
| Industry leading Lowest Total Cost of Ownership | ||
| Bio Banking, eLab Notebook, & Data Management in a single product | ||
| Easily customized in minutes with NO programming | ||
| Easiest and fastest integration with lab equipment | ||
| Complete cross platform support with support for multiple DB’s | ||
| Create complex workflows to track any lab protocol in minutes | ||
| Advanced scheduling system to schedule resources and workflows | ||
| Requires extensive consulting to implement and support | ||
| FDA and GxP Compliant |
Additional Features
Completely Customizable
- Easily extendible with no programming
- Add unlimited new fields and tabs as well as dependent fields for integrated workflows
- Group new fields logically via tabs
- All new fields automatically available in rest of system including batch imports, auditing, reporting and querying
Powerful, Integrated Query Tool
- Powerful and easy to use query tool to interrogate data warehouse contents
- Create and save queries for other users
- Save reports as PDF's, HTML or CSV’s
Compliance and Security
- Secure login authentication
- Object level authority assignment
- Complete field level audit tracking and signing
- Fully compliant with FDA 21 CFR 11


