What is a Clinical Trial Management System (CTMS)?

What is a Clinical Trial Management System (CTMS) ?

Clinical trials are fundamental in advancing medical science, offering new treatments and drugs to improve patient care. However, managing these trials is a complex task involving multiple stages and stakeholders. To streamline this process, Clinical Trial Management Systems (CTMS) have become essential for clinical research sites to organize efficient site management.

Save Our Sites LinkedIn Live: How Is RealTime Working To Save Our Sites?

Save Our Sites LinkedIn Live: How is RealTime Working to Save Our Sites?

In this Save Our Sites LinkedIn Live – How is RealTime Working to Save Our Sites, the organizers of the upcoming Save our Sites conference, caught up with the founders of RealTime, Complion, and Devana Solutions. They discussed how their strategic partnership is reshaping technology in the clinical research landscape. The amalgamation of RealTime, Complion, and Devana signifies a move to consolidate all … Read more

What is eSource in Clinical Trials? Beyond Paper. 

What is eSource in Clinical Trials?

Technological advancements and adoption in clinical trials continue to reshape the way data is collected, managed, and analyzed by clinical research sites, sponsors and CROs. Over the last decade, Electronic Source (eSource) has gained prominence for enabling direct data entry by investigators, reducing transcription errors and enhancing data quality.   eSource in clinical trials is often … Read more

Save Our Sites LinkedIn Live – How Will RealTime Save Our Sites?

Save our sites linkedin live

Built for sites by a site owner, RealTime Software Solutions is designed to help sites overcome some of the top challenges that they’ll face in 2024. In this Save Our Sites LinkedIn Live – How is RealTime Working to Save Our Sites, the organizers of the upcoming Save our Sites conference, caught up with the founders of … Read more

Leading Pediatric Research Center Selects  Complion eRegulatory Platform

Complion eRegulatory platform

SAN ANTONIO, Texas, Jan. 23, 2024 – Complion, LLC, a leader in eRegulatory solutions (eReg and eISF) for clinical trials, is teaming up with a world-renowned pediatric research center. This collaboration signifies a notable achievement for Complion, a RealTime Software Solutions Company, as this esteemed pediatric research center adopts their enterprise-grade eRegulatory platform to ensure … Read more

RealTime Software Solutions Reports Record Growth in 2023, Emerging as the Premier Clinical Trial Management Solution for Clinical Research Sites 

RealTime reports record growth

SAN ANTONIO, Texas, Jan.17, 2024 – RealTime Software Solutions, a leading provider of cutting-edge eClinical solutions for clinical research sites, proudly announces a year of remarkable growth and success in 2023, solidifying its position as the premier choice for clinical research sites navigating the complexities of clinical trials. The company’s success has been amplified through … Read more

Why Your Clinical Research Site Needs More Than a CTMS

Clinical trials require precise management across various domains such as patient recruitment, data collection, regulatory compliance, and stakeholder communication. While Clinical Trial Management Systems (CTMS) have been pivotal in organizing and simplifying many of these aspects for clinical research sites, the complexity of modern clinical research often necessitates a broader array of solutions.   CTMS platforms … Read more

On-Demand Webinar: Mastering FDA Audit Readiness & Easing Site Burden

Mastering FDA Audit Preparedness

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 and Easing Site Burden.” Our panel of experts unpack the potential of eRegulatory solutions in solving common compliance challenges. Check out valuable insights that will help you proactively manage FDA audits and compliance requirements.   What … Read more

Clinical Trial Site Management: A Complete Checklist for Clinical Research Sites

Clinical Trial Site Management

Do you have the right site technology to start studies faster, reduce FDA audit risk and lower protocol deviations? Increasingly, clinical research is transitioning from paper-based processes to the adoption of electronic workflows. In fact, since the FDA’s 2003 draft guidance on electronic technology in clinical investigations, the industry has witnessed a surge in the … Read more

7 Key Takeaways: Mastering FDA Audit Preparedness  

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 that 48% of attendees spend anywhere between 6-10 hours, on average, preparing for an audit. We have a solution for that. We caught up with clinical trial experts Amanda Lesinski, Assistant Director of Regulatory Affairs … Read more