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Centerlinx is a proactive, fully validated clinical trials data management system that provides a seamless technology infrastructure for maximum flexibility in protocol management over a study's life cycle. Delivering solutions for rigorous study demands, Centerlinx is designed to help reduce timelines and provide accurate, real-time clean data.
Features:
Protocol Management
- Unique worldwide accession numbers to simplify sample tracking
- Real-time inspection and auto verification of data for each visit
- Automated ordering of tests per visit/per patient reducing errors and ensuring protocol compliance
- Customized high quality bar-coding requisitions for ease of use on an international basis
- Tracking of expired kits and containers minimizing trial costs
- Multi-level services such as blinding and alert flagging
- 21 CRF Part 11 compliant and complete audit train of all study events
Web Based Access Through Medtrax
- Internet access for report viewing
- Customized reporting by visit and recipient
Electronic Data Transfer
- Dedicated data analyst for format development and query resolution guaranteeing clean data
- Customized electronic format definition and delivery includes ASCII, SAS and Excel files
- Transfer available via diskette, CD-ROM or electronically
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