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Reduce Development Time With the Agile Approach to Bioclinica IRT
To reduce the development time and risk of rework inherent to most IRT systems, we’ve developed a robust core system...
Build and Manage Studies on Your Own with Bioclinica EDC Solo
The Bioclinica EDC Solo delivery model combines the full features and functionality of Bioclinica EDC, which is used by Bioclinica’s...
Ensure High-Quality Data with Bioclinica’s Comprehensive Clinical Data Management Services
Accelerate database lock and gain confidence in the data for your regulatory submissions with full-service Clinical Data Management (CDM) that...
Powerful Clinical Trial Management: A Rapid Startup CTMS
A Clinical Trial Management System (CTMS) is used to centralize data and automate processes for better decision making. Typically, an...
Managing Clinical Supply Chain Risks with the Right RTSM Plus Trial Supply Optimization
The clinical supply chain represents a particular need in clinical trials to synchronize many complex processes and multiple organizations. Without...
Are You Ready for eCTD Submissions?
As of May 5, 2017, the US Food and Drug Administration is only accepting submissions in Electronic Common Technical Document...