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Aims to streamline overall study resource requirements
January 28, 2016
By: Kristin Brooks
Managing Editor, Contract Pharma
Bioclinica has launched a new Post-Approval Research division as part of its Global Clinical Research business segment. Leveraging its technology expertise, the service aims to streamline overall study resource requirements, and is flexible, scalable and customizable. It offers full access to real-time study metrics and transparency for all stakeholders. The Post-Approval Research operates a Program Coordinating Center (PCC) with dedicated research staff and provides global operational infra...
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