LiRAS® for LiPA® Cystic Fibrosis
Objective reading and interpretation of INNO-LiPA® strips for detection of CFTR mutations and wild-type.
The LiRAS for LiPA Cystic Fibrosis software assists you in the interpretation of CF typing results.
Note: For automated scanning of test results, a flatbed scanner of a specific type is required. For more information on the latest supported scanners pleace contact us.
Product number 80535
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Details
Features & Benefits
- Audit trail and revision history for full traceability
- Scanning with integrated calibration: to ensure accurate interpretation
- Reporting options: customize your reports and insert your own logo
- Filter management: define your own queries and obtain quick overviews
- User management: assign user privileges for your laboratory personnel
- Allows the use of electronic signatures for Test review and Approval
- Can be connected to a Laboratory Information Management System* (LIMS): import worklists from, and export results to, your LIMS system
- Manual in 8 languages
*NB: This requires intervention of the LIMS provider
System requirements- Microsoft Windows XP, Windows 7, Windows 8 and Windows 10 Operating System
- 1Ghz Processor
- 500 MB free Hard Disk Space (recommended: 2 GB or more)
- 2 GB RAM (recommended: 4 GB or more)
- Minimum Screen Resolution: 800 by 600 pixels
- USB 2.0 is recommended.
Disposables:- LiPA-Scan reading template (pack of 25) (art nr. 80350)
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Conditions of sale
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Documentation
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Insights
Early, easy, efficient and cost-effective diagnosis of Cystic Fibrosis
Cystic Fibrosis is one of the most frequent life threatening inherited diseases. If detected early, effective treatment can be started improving...
Nov 28, 2019
Cystic Fibrosis, diagnosis and molecular testing
Cystic fibrosis (CF) is one of the most frequent human genetic disorders, predominantly affecting individuals of Caucasian descent in North America...
May 22, 2019
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