7 Key Takeaways: Mastering FDA Audit Preparedness
In Mastering FDA Audit Preparedness: Streaming Compliance and Easing Site Burden, a webinar hosted by Complion, an audience poll revealed
In Mastering FDA Audit Preparedness: Streaming Compliance and Easing Site Burden, a webinar hosted by Complion, an audience poll revealed
Study startup and site activation are key to the clinical trial process, but often suffer from delays. It can be
Regardless of size and type, clinical research site organizations compete for trial opportunities from CROs and sponsors. There are many
According to a review from the National Library of Medicine, clinical trials can fail for many reasons. Among the top
In March 2023, the FDA issued an update to its Electronic Systems, Electronic Records, and Electronic Signatures in Clinical Investigations
Are your clinical trials ready for an audit, inspection and/or site monitoring visit now? If your organization is running clinical
Clinical trial inspections, monitoring visits, and audits are all important quality assurance measures that are used to ensure the integrity
In the ever-evolving field of clinical research, technological advancements continue to revolutionize how we conduct studies and collect data. One
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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