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