Save Our Sites LinkedIn Live: How Is RealTime Working To Save Our Sites?
February 6, 2024
In this Save Our Sites LinkedIn Live – How is RealTime Working to Save Our Sites, the organizers of the upcoming Save our
What is eSource in Clinical Trials? Beyond Paper.
February 6, 2024
Technological advancements and adoption in clinical trials continue to reshape the way data is collected, managed, and analyzed by clinical
Save Our Sites LinkedIn Live – How Will RealTime Save Our Sites?
February 1, 2024
Built for sites by a site owner, RealTime Software Solutions is designed to help sites overcome some of the top
Why Your Clinical Research Site Needs More Than a CTMS
January 17, 2024
Clinical trials require precise management across various domains such as patient recruitment, data collection, regulatory compliance, and stakeholder communication. While
On-Demand Webinar: Mastering FDA Audit Readiness & Easing Site Burden
January 12, 2024
https://vimeo.com/898629213?share=copy Webinar Date: October 25, 2023 Discover the keys to audit readiness in webinar, “Mastering FDA Audit Preparedness: Streamlining Compliance
Clinical Trial Site Management: A Complete Checklist for Clinical Research Sites
January 11, 2024
Do you have the right site technology to start studies faster, reduce FDA audit risk and lower protocol deviations? Increasingly,
7 Key Takeaways: Mastering FDA Audit Preparedness
December 27, 2023
In Mastering FDA Audit Preparedness: Streaming Compliance and Easing Site Burden, a webinar hosted by Complion, an audience poll revealed
Expedite Your Study Startup – A Site Checklist
November 16, 2023
Study startup and site activation are key to the clinical trial process, but often suffer from delays. It can be
