Centerlinx
Centerlinx is a proactive, fully validated clinical trials data management system that provides a seamless technology infrastructure for maximum flexibility in project management over a study's life cycle. Delivering solutions for rigorous study demands, Centerlinx is designed to help reduce timelines and provide clean, accurate, real-time data.
FEATURES
Project Management
- Unique accession numbers to simplify specimen tracking, especially for global studies
- Real-time inspection and automated verification of demographics and other data for each protocol visit
- Automated test ordering options for each patient visit, reducing errors and helping to ensure protocol compliance
- Study-specific, bar-coded requisitions for ease of use on an international basis
- Tracking of expired specimen collection kits and containers to minimize trial costs
- Multilevel services such as blinding and alert flagging
- 21 CRF Part 11 compliant, with a complete audit trail of study events
- Report viewing available via a secure Internet connection
- Options for customized reporting by visit and patient
- Dedicated data analyst for format development and query resolution
- Flexibility in data formats, including ASCII, SAS, and Excel files
- Data transfer available electronically or via disk or CD