Allows the “Medical Writer” to save time by reusing standard content to produce accurate documents through the Protocol Automation feature
Ensures effective tracking of the volunteer's life cycle from registration to end of clinical trial with biometrics through the Volunteer Management feature
Offers a Simple & Easy tracking of sample movement with no data loss
Product Highlights :
Interactive analytical dashboard customizable to user/role
Customizable predefined templates to auto generate documents effectively in quick time meeting the quality requirements
Fully digitized authoring and approval structure for the entire document cycle
Collaboration of multiple users with controlled access and built-in workflows
Pre-screening of volunteers & ID card generation with barcoding feature for tracking
Volunteer registration to subject sample collection life cycle tracking
Easy to export & attach documents
Fully compliant system to meet Industry guidelines with highly secure data
