Clinical Trials
The LabPas CT (Clinical Trials) module automates the management of early phase clinical data sample processing and operational workflow.
With LabPas CT you can:
- Set up a study in hours rather than days using adaptable data elements
- Capture data directly by deploying wireless mobile devices at point-of-subject to scan subject, dose, collection vessel and instrument barcodes, using the LabPas CT Mobile interface
- Capture real-time electronic data for collection times, comments, dosing, vital signs and adverse events
- Manage adverse event observations and create electronic adverse event forms
- Set up configurable edit checks, cleaning data as it is entered
- Share real-time data with investigators and sponsors, using the LabPas Data Qualification interface
- Raise and resolve data queries
- Report data via standardized reports, ad hoc reports and in CDISC ODM format
LabPas Customer Support:
Phone: 866-522-7271 or 802-223-9800
Then select Option 3
Fax: 802-262-1065
E-mail Address: labpas.support@phaseforward.com
