Lūg Trials: Management System for Clinical Trials
LŪG Trials provides a control framework enabling an exhaustive control of all the steps that are carried out in the processes of preparation, development and reporting of a clinical trial, covering both documentation tasks and drug management.
Lūg Trials provides integral traceability for:
- Documentation
- Participants / Recruitment
- Drug / Kit Number
- Handling / Temperature Monitoring
- Production
- Quality Control / Certification
- Administration
Lūg Trials provides comprehensive control over clinical trials processes at the hospital pharmacy, preventing delays and decreasing unnecessary costs on drug destruction and also involved personnel travel expenses, covering the entire documenting tasks, from administration to patients, through other areas involved in the process, such as production (i.e. at sterile facilities) or dispensation (i.e. oral treatments).
Special emphasis to achieve on all the critical issues, including temperature monitoring, gravimetrical and identification controls, etc.; all data produces is stored in the traceability database, that becomes a priceless knowledge database.