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
At the 2022 Drug Information Association Annual Meeting, held in-person in Chicago June 20-23, representatives from the compliance offices of the FDA and MHRA gave a detailed assessment of the pros
Adapted from a Phlexglobal Ask An Expert interactive discussion held May 11, 2022 and available on-demand here. Why Integrate Your CTMS and eTMF Systems? A typical electronic Trial Master File
Read the latest blog from our Pharmalex colleagues, Milena Shuytsova-Mircheva and Lisa Pascoe, who discuss the benefit of the Clinical Trial Information System (CTIS). Companies have one year to
Phlexglobal provides a unique Trial Master File solution by leveraging dedicated and authoritative TMF technologies and expert services to bring order, stability, and control to your Trial Master File – helping you achieve the highest standards for completeness, timeliness, and quality.
UK: +44 (0) 1494 720420
US: +1 (484) 324-7921
E-Mail: info@phlexglobal.com