Faster time to approval
Optimized revenue opportunities
Increased efficiency and accuracy
Improved planning and tracking of regulatory activities
Faster, more accurate Health Authority communications
Global compliance with current and future needs
Registration planning, tracking and management built for both your data and automation of your key processes.
A single regulatory database that will help you to avoid redundant data that exists within your submissions.
Migrating Trial Master File (TMF) data is a fairly common occurrence, usually driven by one or more of the following scenarios: Implementing a new electronic Trial Master File (eTMF) system
Based on extensive work helping trial sponsors and Contract Research Organizations (CROs) implement Trial Master File (TMF) best practices, Phlexglobal’s experts repeatedly encounter teams struggling
In a poll of nearly 100 TMF professionals during a recent Phlexglobal webinar, “Lowering your TMF Risk Temperature: Real-world Use Cases and Lessons Learned,” more than half of the respondents were
UK: +44 (0) 1494 720420
US: +1 (484) 324-7921
Poland: +48 81 45 46 132
Germany: +49 89 23514741
E-Mail: info@phlexglobal.com