An analysis published in the National Library of Science identified that key drivers for start-up delays in clinical trials include
eRegulatory, often abbreviated as eReg or eReg/eISF (electronic investigator site file), refers to the use of electronic systems to manage
A clinical research site’s study pipeline is tied to its overall performance, with CROs and sponsors rewarding sites that demonstrate
The evolution of data collection and management in clinical trials has seen a significant shift from traditional paper-based methods to
An interview with Phillip Stanford, Senior Director, Applications & PMO at EmVenio Research, a PCM Trials Company. Q: Can you
As clinical research organizations grow, many tasks can become siloed and the overall lack of transparency can lead to inefficiencies,
Study start-up and pipeline management are fraught with challenges that can hinder progress and efficiency. These complex processes involve meticulous
At the center of every clinical trial lies a maze of regulatory requirements, from FDA regulations to institutional review board
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