Clinical trial automation software at DIA


Preparing for CDISC standardized electronic submissions.

Celebrating the launch of the “Convert datasets” service, and 16 years of CDISC expertise, Formedix is well placed to help organizations prepare for regulatory change. Join CDISC experts on booth #2434 to discover how Formedix can help you prepare for the FDA’s regulatory deadline for CDISC standardized electronic submissions imposed in December 2016. Armed with revolutionary software, services and an extensive range of training, it’s sure to be an exciting time on the Formedix booth.

“We look forward to exhibiting at the DIA show each year, more so this year due to our exciting new releases,” said Jason Chan, Solutions Consultant at Formedix. “This year sees the FDA impose regulations for CDISC standardized submissions, making it increasingly difficult for organizations to reach submission and remain regulatory compliant. At Formedix we are committed to automating manual and time consuming tasks across the clinical trial process and we are advocates of early implementation of CDISC standards. The latest additions to our toolkit significantly reduce the challenges faced by organizations and provide proven time and cost savings.”

“DIA is a great opportunity to see the latest technologies and trends and I’m confident that Formedix solutions won’t disappoint.”

Join Formedix on booth #2434 at the meeting in Philadelphia, PA, for a glimpse of the new automated Convert Datasets service in action.


Book a booth appointment with our CDISC experts to leverage our experience of CDISC standards and FDA submissions.