PCT in Vienna, Austria, 19-21 November 2013

We are driven by a mission to make a meaningful impact in the Life Sciences industry. We provide flexible e-Clinical software systems for Clinical Research Organizations (CROs) and pharmaceutical companies worldwide.   Key Responsibilities  Requirement Gathering & Documentation:  Collaboration & Communication:  Process Improvement & Mentorship:  Client Engagement:  Typical Tasks:  Formalizing change requests from customer consultations into […]

CDISC is introducing TMF Standard Model V1, the next evolution of the widely used TMF Reference Model. This is more than a new version – it represents a shift toward standardized, digitally managed clinical trial records. What’s changing? When will it happen? Community review of the draft is scheduled to begin this autumn, with the […]

When vendors build tools to evaluate TMF health, they usually focus on three main KPIs: completeness,  timeliness and quality.  These metrics are obviously important, but are they enough?  A real TMF user will go further and ask the next question:  How long did it take the document to move through each of these stages?  The […]

We’re proud to share a milestone with our partners at Astrum: the first phase of their Flex Databases implementation is now live.Project management and project time tracking now run in one shared system. Here’s what changes:– Operational teams log their time directly in Flex – no more local tools or Excel-based tracking– Project managers plan […]