Phlexglobal is the leading technology and services organization for clinical and regulatory matters with a focus on helping clients to master their digital agenda via proven AI solutions. Phlexglobal combines software and leading expert services to offer a unique solutions portfolio with easy to achieve automation via data generation that lifts organizations to a new level of effectiveness.
PhlexTMF, the company’s Trial Master File software, and Regulatory Solutions including PhlexSubmission for eCTD and CTD, PhlexIDMP, PhlexEVMPD, and PhlexRIM are considered highly innovative in the industry for their out of the box best practices capabilities. use of automation technology and user-focuses design.
PhlexDistiller, a machine learning platform that reads documents and converts unstructured content into structured data, achieves automation of regulatory and clinical processes and completes the end to end solutions offering from Phlexglobal.
Own the situation
--regardless of who
is delivering it
or who caused it.
There are no stars in the room.
Side before self -- every time.
Give it a go.
Be visible
Fulfill your promises.
Take cabinet responsibility.
Be transparent on progress.
Focus on the end game.
Celebrate victories.
Industry expertise, technological vision, and operational authority combined into one team.
Resources ready to help improve your TMF processes, technology, and people.
Bring your expertise and passion to the TMF Authority for a rewarding career in clinical trial management.
Have a question? Interested in a demonstration? Let us know and we'll be in touch.
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
