Regulatory Updates in Clinical Trials: What’s New
In 2025, clinical research will continue to undergo significant transformation driven by key initiatives and updates from regulatory authorities like
In 2025, clinical research will continue to undergo significant transformation driven by key initiatives and updates from regulatory authorities like
2025 is set to bring new advancements in clinical trial site management driven by technology, efficiency demands, and industry growth.
Sponsors are raising their expectations for clinical research sites to deliver higher levels of efficiency, data integrity, compliance, and patient
At the recent Decentralized Trials & Research Alliance (DTRA) conference, industry leaders took to the center stage to discuss one
Electronic Source (eSource) presents a compelling case for reducing monitoring costs in clinical trials. By streamlining data collection, improving accuracy,
This webinar served as a call to action for the industry, emphasizing the need for collaboration, transparency, and innovation to make clinical research a more inclusive and effective care option.
Clinical research is highly competitive and regulated. Staying on top of study oversight and management is crucial for research sites
The adoption of eReg/eISF solutions in clinical trials can significantly improve outcomes across Academic Medical Centers (AMCs) and health networks,
RealTime eClinical Solutions is a leading, enterprise-grade technology provider facilitating global clinical trials with a comprehensive eClinical platform. Purpose-built for clinical research sites, site networks, academic medical centers, sponsors, and CROs, the platform goes beyond traditional CTMS to empower research and business workflows for modern-day clinical trials.
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