TrackWise provides organizations with a fully electronic, web-based tracking solution that tracks, manages, and controls all clinical trials processes and tasks through a consolidated dashboard and desktop view. TrackWise is a web-based enterprise quality management software solution that enables your organization to comply with 21 CFR Part 11, GMP, GLP, GCP, and other industry standards.
FEATURES:
- Streamline the clinical trials process by consolidating tracking and management of all clinical trials activities into an easily accessible web-based system.
- Increase resource utilization and collaboration by automating workflow processes and providing secure access to related information across multiple sites, studies, teams, and trials.
- Reduce risk of lost records, incomplete items, and overdue tasks by eliminating paper and tracking items electronically.
- Increase visibility of pending items through on-line reporting and dashboards.
- Reduce administrative costs and duplicate efforts by leveraging TrackWise's 24/7 business rules engine, which automates manual procedures and escalates commitments based on priority, due date, and other criteria.
- Improve the effectiveness of monitoring visits by utilizing on-line inspection checklists and questionnaires and tracking any violations or discrepancies through completion.
- Improve the evaluation adverse events, minimize data entry errors, and streamline the creation and tracking of serious adverse events (SAE) reports.
- Improve visibility of product safety issues and streamline the regulatory assessment and reporting process for SAEs.
- Access distributed documentation through integrated document management technology, or by integrating to your existing document management system.
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