This integrated approach allows multiple partners and stakeholders to collaborate under one unified and regulatory compliant platform.
Better ability to meet trial timelines with improved site performance.Savings of up to 55% in site-monitoring costs.A reduction in SDV between 45% to 65%.
Webinar1 - New Metadata Role for LifeSciences and Healthcare
Date:September 30, 2015
Webinar2 - Data Sciences - The New Analytics Paradigm
Date: October 8, 2015
Study Design - Plan Collaboratively and Deploy Efficiently
Clinical Data - Collect, Manage, Analyze, Review in Integrated and Metadata Driven Platform
Clinical Portfolio - Managed Prospectively and Optimized in Time
Regulatory Submission - Qualitative, On time and Compliant to Global Regulatory standards