Precision, efficient collaboration and control are paramount when managing clinical trials and preparing documents for regulatory agencies. Litéra’s solutions provide the content integrity assurance necessary when meeting tight deadlines for documentation delivery and developing intellectual property.
- Accelerate clinical trials through web-based collaboration tools
- Speed site document exchange of reg-pack, feasibility, SUSARs and other communications with automated distribution, tracking and e-Binder
- Manage training and certification online
- Streamline trial processes with automated workflows and tools for operations staff
- Facilitate planning with automated real-time, transparent reporting of trial status
- Control content of regulatory document submissions
- Collaborate simultaneously on a document, with full auditability
- Clean potentially damaging hidden data from documents
Litéra® is a registered trademark of Litéra Corp. All other brand names, product names, or trademarks belong to their respective holders.