by Mednet | Oct 7, 2026 | Blog
Clinical trial growth isn’t just about running more studies. It’s about managing more complexity within each one. More data sources. More sites. More sophisticated protocols. More systems. And more pressure to move all of it faster. Traditionally, every additional...
by Mednet | Oct 5, 2026 | Webinars
October 14, 2026 at 11 am ET Manual transcription of patient health records into EDC forms has always been a source of frustration for site users and a heavy workload for clinical research associates. While traditional EHR-to-EDC integrations exist to automate this...
by Mednet | Sep 28, 2026 | Blog
Accurate data capture is at the heart of every successful clinical trial, it is also one of the most time-consuming aspects of the operation. Sites are under pressure to capture data accurately and on time, while data managers and monitors continue to spend valuable...
by Mednet | Sep 15, 2026 | Blog
For years, clinical research has relied on a frustratingly manual process: patient information is captured in the hospital’s electronic medical record (EMR) or electronic health record (EHR), then entered again into the electronic data capture (EDC) system....
by Mednet | Aug 31, 2026 | Blog
First Patient In (FPI) is the moment a trial stops being a plan on paper and starts generating real data. It’s also one of the clearest indicators of how efficiently a sponsor or CRO can move from protocol approval to execution. That efficiency is getting...
