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...
by Mednet | Jun 15, 2026 | Blog
In a market where sponsors often evaluate multiple CROs with similar therapeutic expertise, operational capabilities, and geographic reach, differentiation can be difficult. Increasingly, one of the factors that separates CROs is the technology ecosystem they bring to...
by Mednet | Apr 13, 2026 | Blog
What is a unified eClinical platform? A unified eClinical platform is a single, integrated system that manages the multiple aspects of a clinical trial – such as EDC, eConsent, CTMS, and RTSM – within one environment. Instead of stitching together multiple vendors,...
