Leading CRO Chooses RealTime eClinical Solutions for Regulation Management
RealTime eClinical Solutions has made headlines with a significant selection from a leading Contract Research Organization (CRO), chosen for its eRegulatory platform to enhance regulatory document management across hundreds of studies and investigator sites on a global scale.
This important decision signals a growing trust in RealTime's comprehensive solutions, complementing endorsements from three of the top five CROs and nine of the top ten site networks that already leverage RealTime's technologies to boost their operations.
Benefits of RealTime's eRegulatory Platform
As the demands of clinical trials evolve, global CROs are moving away from outdated systems, including cumbersome paper binders and legacy tools that fall short of modern standards of inspection readiness and operational visibility.
RealTime's eReg/eISF platform presents a highly efficient solution by providing a centralized, secure environment. It ensures that all stakeholders—from investigators to monitors—can access the most up-to-date, compliant documentation in real time. With features like automated version tracking, expiration alerts, and complete audit trails, CROs can maintain continuous oversight of their operations without the need for manual processes, fostering readiness and confidence across hundreds of trials.
CEO Stephen Johnson’s Vision
Stephen Johnson, CEO of RealTime eClinical Solutions, emphasized the platform’s capability: "Our eRegulatory platform was built to meet the demands of global, multi-site trials where precision, visibility, and compliance are critical. Being selected by one of the world's largest CROs reinforces what our partners already know; RealTime scales with the industry's most complex operations."
RealTime's platform is trusted by more than 85,000 studies and over seven million patients worldwide, showcasing its effectiveness:
Key Performance Improvements
- Achieving inspection readiness five times faster via centralized documentation and automated workflows.
- Reducing monitoring visit costs by up to 75% through remote document access and real-time visibility.
- Accelerating study start-up with streamlined delegation and signature workflows.
Award-Winning Innovation
Recently, RealTime was honored with the Clinical Trials Excellence Award for Innovation in Digital Platforms, which recognizes its pivotal role in revolutionizing connected clinical trial technology. This accolade highlights the company's ongoing commitment to building systems that merge the business and science aspects of research, from initial study setup through execution and completion.
Johnson added, "RealTime's growth reflects a fundamental shift in how the industry approaches technology adoption. The organizations leading the future of clinical research aren't merely adopting more tools; they are adopting systems that integrate every aspect of the process. That's where RealTime leads."
About RealTime eClinical Solutions
RealTime eClinical Solutions is transforming site-based clinical trials through its comprehensive eClinical platform, which serves as a unified Site Operations Management System (SOMS). This platform seamlessly integrates CTMS, Devana, eSource, eReg/eISF, participant engagement, payments, and analytics into a single ecosystem designed for modern clinical trial operations. RealTime provides sponsors and CROs with unparalleled visibility with TrialAlign, an advanced site selection and feasibility analytics platform. Trusted globally, RealTime enables research organizations to work faster, smarter, and collaboratively.
Media Contact:
Daenya Garcia
Senior Director, Marketing & Communications
(210) 852-4310 x1114
Frequently Asked Questions
What is RealTime eClinical Solutions?
RealTime eClinical Solutions is a company specializing in clinical research software technology designed to improve the operational efficiency of clinical trials.
What platform did the leading CRO select from RealTime?
The leading CRO selected RealTime's eRegulatory (eReg/eISF) platform to streamline their regulatory document management.
How does RealTime enhance regulatory oversight?
RealTime enhances oversight by providing a centralized, secure environment for accessing up-to-date compliance documentation in real time.
What are the main benefits of using RealTime's platform?
The platform offers faster inspection readiness, reduced monitoring costs, and accelerated study startup through efficient workflows.
What recent recognition did RealTime receive?
RealTime received the Clinical Trials Excellence Award for Innovation in Digital Platforms, acknowledging its impactful role in advancing clinical trial technology.
