by Mednet | Nov 2, 2026 | Blog
That pressure is felt across the trial lifecycle, but perhaps nowhere more than in study startup. The startup phase is one of the most resource-heavy and time-consuming parts of any trial. Sponsors expect CROs to constantly look for ways to move faster, reduce burden...
by Mednet | Nov 2, 2026 | Blog
For pharmacovigilance teams, few deadlines carry more weight than expedited safety reporting. When published literature identifies a serious and reportable adverse event associated with a marketed product, regulatory agencies such as the FDA and EMA require...
by Mednet | Oct 15, 2026 | Blog
For pharmacovigilance teams, keeping pace with the growing volume of safety-relevant literature is an ongoing challenge. Once a product reaches the market, thousands of new publications, case reports, conference abstracts, and medical journals become...
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 | 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....
