RealTime eClinical Solutions

Is your clinical trial at risk of a regulatory nightmare? Don’t let regulatory mistakes creep up on you! In this upcoming webinar, we’ll uncover real-life eReg/eISF "horror stories" that can cause terrifying delays and costly compliance issues for clinical trials. Join us on October 30 to learn how you can avoid these frightening pitfalls and keep your trials audit-ready with the right eReg/eISF solutions. 📅 Webinar: eReg/eISF "Horror Stories" – Avoid Regulatory Pitfalls & Costly Delays October 30 | 12 PM ET What You’ll Learn: -How to avoid getting spooked by monitor queries with a clean audit trail. -The scary costs of outdated or expired documentation. -How to speed up study start-up and reduce the burden of signature collection. -The ROI of switching to electronic signatures and the time you’ll save. 🔗😱 Don’t let your trials turn into a regulatory nightmare! Can’t make the live event? Register now and save your spot. https://lnkd.in/gwBmTmy6 #ClinicalTrials #eRegulatory #Compliance #AuditReady #Webinar #ClinicalResearch #HalloweenWebinar #RegulatoryHorrorStories

AMCs and health networks face significant challenges in maintaining operational efficiency, data integrity, and regulatory compliance. One pivotal strategy to navigate this challenging environment is the effective capture and tracking of key performance metrics. These clinical trial performance metrics offer vital insights that can guide AMCs in fine-tuning their trial processes and achieving better outcomes. However, the task of managing these metrics can often become overwhelming. Enter RealTime-Devana, a purpose-built platform designed to simplify the clinical trial process by capturing, displaying, and optimizing key clinical trial performance metrics throughout the entire trial lifecycle. Whether the trials are investigator-initiated, grant-funded, or industry-sponsored, Devana provides true end-to-end visibility and operational oversight that allows research organizations to operate more efficiently and make informed, data-driven decisions.  👉 Keep reading: https://lnkd.in/gvcbhafH #trialperformance #dataanalytics #clinicaltrials #clinicalresearch #Devana

🔍Clinical trials demand pinpoint accuracy and strict adherence to regulations. While Electronic Health Records (EHRs) are essential for patient care, eSource is engineered specifically for the unique complexities of clinical trial data management. Understanding the difference between these technologies can significantly impact trial outcomes. Check out this resource to unpack the key differences between eSource vs EHR/EMR. 🎯 Purpose EHRs: Focus on managing patient care and medical histories across healthcare settings. eSource: Tailored for managing clinical trial data, ensuring every detail meets protocol standards. 🛠️ Functionality eSource: Boosts trial accuracy with reduced errors, real-time data updates, and solid audit trails. EHRs: Great for general healthcare management but not built for the specific demands of clinical trials. 🔗 Read the complete details here: https://lnkd.in/ge6Yhiwh #ClinicalTrials #eSource #InnovativeSolutions #DataManagement #ClinicalResearch

Clinical trials have been undergoing a monumental shift as sites, AMCs, sponsors, and CROs move away from traditional paper-based and disparate systems towards more integrated, and efficient eClinical systems. Our latest blog delves deep into how this evolution is driven by the increased adoption of eRegulatory systems, which streamline the management of regulatory documents and processes digitally. Learn about the pivotal trends propelling this change and how they're setting the stage for a future where clinical trials are more efficient, compliant, and technology-driven. From improving data integrity to enhancing real-time monitoring capabilities, eRegulatory systems are at the heart of modernizing clinical research. 👉 Dive deeper into our discussion and discover the five key trends shaping the future of clinical trials. Read the blog here: https://lnkd.in/gr9wMD5V #ClinicalTrials #eRegulatory #eClinicalSolutions #InnovativeSolutions

We’re counting down to the 2024 AACI/CCAF Annual Meeting, October 20-22. RealTime, with Devana, supports cancer center leader and administrators by offering real-time performance metrics and end-to-end visibility. Devana empowers cancer centers with crucial business intelligence, improved project management, and accelerated study timelines—all essential for advancing research and patient care. Barry Lake and Michael Bonavilla will be there to help you explore how Devana can drive efficiency and improve outcomes for your center. We can’t wait to meet you! Let’s connect at spot #7! https://lnkd.in/eRue8b8i #AACICCAF #ClinicalResearch #CancerCenters #RealTimeCTMS #DevanaSolutions #InnovationInResearch #LetsConnect

TIPS & TRICKS: Clinical Trial Data Analysis 𝑪𝒉𝒐𝒐𝒔𝒆 𝒘𝒉𝒂𝒕 𝒄𝒍𝒊𝒏𝒊𝒄𝒂𝒍 𝒕𝒓𝒊𝒂𝒍 𝒅𝒂𝒕𝒂 𝒚𝒐𝒖 𝒘𝒂𝒏𝒕 𝒕𝒐 𝒔𝒆𝒆, 𝒆𝒙𝒂𝒄𝒕𝒍𝒚 𝒉𝒐𝒘 𝒚𝒐𝒖 𝒘𝒂𝒏𝒕 𝒕𝒐 𝒔𝒆𝒆 𝒊𝒕. → While RealTime-Devana's default dashboards feature all the core trial-related information for your organization, you can drill down even further with custom report and visualization options. → Devana automatically captures overall performance metrics both within the platform and via integrations with other systems such as CTMS, allowing for full-cycle data display and analysis. In fact, every data point captured within Devana is reportable. → With all the necessary data at your fingertips, you can easily monitor emerging trends, identify struggling sites, and make more informed decisions. Devana also makes it easy to subscribe to reports for the latest updates and to share actionable insights with internal and external stakeholders alike. Learn more about how Devana can transform your clinical trial processes with advanced data analytics: https://lnkd.in/gpXEBv4t #dataanalysis #clinicaltrials #clinicalresearch #Devana

𝑵𝒐𝒕 𝒂 𝒇𝒂𝒏 𝒐𝒇 𝒕𝒚𝒑𝒊𝒏𝒈 𝒐𝒏 𝒚𝒐𝒖𝒓 𝒑𝒉𝒐𝒏𝒆 𝒐𝒓 𝒕𝒂𝒃𝒍𝒆𝒕? Using the voice dictation feature in RealTime-eSource will help you avoid this and save time. Instead of typing up source notes, simply speak directly into the RealTime Mobile App on your phone or tablet and it will automatically be transcribed into your source database! 🔗 Learn more about this and other helpful eSource features here https://lnkd.in/gb4S4A9q #eSource #BetterResearch #BetterData #InnovativeSolutions #clinicaltrials #clinicalresearch

Are you still relying on paper-based data collection to run your clinical trials? Clinical research sites, AMCs, and health systems are all moving away from paper-based methods and adopting eSource for one key reason: it makes their trials more efficient and accurate. Here's how: → Say so long to transcription errors! eSource captures data directly at the source, ensuring real-time accuracy and reducing the need for manual entry. → Streamline your document and signature collection, speeding up study initiation and keeping your trials moving forward. → eSource provides automatic audit trails and real-time data tracking, making it easier to stay compliant and audit-ready at all times. → Access trial data from anywhere, anytime, and monitor trials in real-time without the need for constant on-site visits. Explore how eSource can save time, reduce errors, and improve efficiency right here: https://lnkd.in/gB2C-yHE #eSource #ClinicalTrials #DataManagement #Compliance #eClinicalSolutions #ClinicalResearch #RealTime

 🏆 We're so proud and thrilled to share that our very own Rick Greenfield, Founder and Chief Strategy Officer at RealTime eClinical Solutions, has been awarded a Lifetime Achievement Award at the 2024 Society for Clinical Research Sites (SCRS) Global Summit! With over two decades of experience in the clinical trials industry, Rick has been a driving force in improving site operations through cutting-edge technology and unwavering support for clinical research sites. His leadership and vision have led to the development of some of the most impactful site-based eClinical solutions available today, including RealTime’s flagship CTMS, eReg/eISF, eSource, and participant engagement tools - solutions that empower sites to streamline workflows, strengthen compliance, and ultimately deliver improved trial outcomes. Rick’s drive for innovation, combined with his dedication to site success, has transformed how research is conducted across thousands of sites worldwide, leaving a lasting legacy in the industry. This award is a well-deserved recognition of his contributions. 👏Congratulations, Rick! #SCRS2024 #LifetimeAchievementAward #ClinicalResearch #Leadership #eClinicalSolutions #InnovativeSolutions

𝐓𝐨𝐝𝐚𝐲’𝐬 𝐭𝐡𝐞 𝐝𝐚𝐲! Join us for an SCRS hosted webinar on the future of hybrid clinical trials - Standardizing Scalable and Compliant Technology for Hybrid Trials. In this webinar, explore how technology supports increasing diversity and access to clinical trials by streamlining operations, centralizing trial data, and providing real-time access for more efficient trials. This is a must-attend event for anyone looking to drive better outcomes and create more inclusive and accessible trials. See you there!   🎙 Featuring Industry Experts: Rick Greenfield, Founder & Chief Strategy Officer, RealTime Phillip Stanford, Senior Director, Applications & PMO, EmVenio Research   🔗 It’s all happening today—see you there! 💻✨Free for SCRS Members. https://lnkd.in/g5R2ZmU6   #ClinicalTrials #HybridTrials #Webinar #DEI #RealTimeData #TrialEfficiency #ClinicalResearch #InnovativeSolutions #SCRS