With our recent brand refresh, we introduced a new tagline that embodies our brand promise. While we emphasize AI, our technology is designed for the humans running the trials. We’re not just about data—we’re about making a difference. Our cutting-edge software empowers people to work faster and smarter, enabling them to improve even more lives worldwide. 🌍 As innovators at heart, we harness advanced statistics and machine learning to transform data into positive outcomes for clinical development. Ready to join the revolution? Let’s make magic happen together! 🎩✨ https://hubs.ly/Q02FVqHH0 #RBQM #RiskBasedQualityManagement #ClinicalTrials #DataQuality
About us
CluePoints is the premier provider of RBQM and data quality oversight software. We’re leveraging the potential of AI using advanced statistics and ML to determine the quality, accuracy, and integrity of clinical trial data both during and after the study. Aligned with guidance from the FDA, EMA, ICH, and MHRA, CluePoints supports central and on-site monitoring, medical review, and quality risk management to drive a holistic risk-based strategy. Coupled with thought leadership and consulting expertise to aid risk assessment and solution implementation, the result is positive clinical development outcomes, increased operational efficiency, lower costs, and reduced regulatory submission risk as part of the industry paradigm shift to RBQM. To learn more about CluePoints, visit CluePoints.com.
- Website
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https://cluepoints.com/
External link for CluePoints
- Industry
- Software Development
- Company size
- 201-500 employees
- Headquarters
- Avenue Albert Einstein 2A, Louvain-La-Neuve
- Type
- Privately Held
- Founded
- 2012
- Specialties
- Central Statistical Monitoring, Risk-Based Monitoring solutions, risk-based quality management, and ICH E6 (R2)
Locations
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Primary
New Tech Centre
Avenue Albert Einstein 2A, Louvain-La-Neuve 1348, BE
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1000 Continental Dr
Suite 240
King of Prussia, Pennsylvania 19406, US
Employees at CluePoints
Updates
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🔥 The countdown is on! #RBQMLive is your ticket to transforming clinical trials. Gain exclusive insights, network with industry leaders, and stay ahead of the curve. Don’t wait – register today and be part of the revolution 👉 https://hubs.ly/Q02HF-k40
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🎉 Get ready for an action-packed kickoff to RBQMLive! Day 1 is set to bring you incredible sessions, with topics on RBQM adoption, industry guidance evolution, and AI/ML innovations. Don’t miss the latest industry trends and collaborative discussions. Register now: https://hubs.ly/Q02HFNsq0 #RBQMLive2024 #RiskManagement #ClinicalTrials #September2024
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Our ultimate guide to RBQM is here to save the day! 🦸♂️✨ Say goodbye to trial headaches and hello to smart, efficient research. Dive into the history and implementation , and master best practices—all in one comprehensive resource. Grab your copy now and step into the future of clinical research: https://hubs.ly/Q02FbnqW0 #RBQM #ClinicalTrials #ClinicalResearch #DataQuality
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Change up how you're doing things. See results. 🧪 Our new infographic reveals how RBQM is transforming CRO compliance and risk management. From proactive risk handling to meeting ICH and FDA guidelines, we have the ingredients for smarter, faster trials. Big or small CRO, our AI-driven solutions make the difference. Curious? Dive in:👉 https://hubs.ly/Q02HwxHm0 #RBQM #ClinicalTrials #CROs #ClinicalResearch #RiskManagement
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🔥 Buckle up! Our RBQM enhancements have landed, and they’re game-changing. Our latest features are designed to supercharge your RBQM and Data Review experience. Here’s a look at what’s new: 🔍 Audit Trail Review (ATR) functionality to analyze trial metadata in great detail 🎨 Enhanced UX and killer visuals on both KRI and QTL Dashboards 🔗 Integrated Risk Assessment & Mitigation modules to streamline processes 📊 Unified feed to modify risk origin, generate new signals, and monitor all user activity ⚡ Rapid setup for clinical and operational data ingestion and processing Ready to elevate your clinical trials? Contact us to get started: https://hubs.ly/Q02Fbmv_0 #RBQM #RiskBasedQualityManagement #ClinicalTrials #ClinicalResearch #DataQuality
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📢 Exciting announcement! Olivia Feiro, Director of Risk Management & Analytics at CSL Behring, will be joining us at RBQMLive 2024. She’ll be speaking on the panel “RBQM Industry Guidance Evolution – Adapting to Modernization.” Discover opportunities and challenges with evolving guidance, strategies for integrating quality by design, and approaches to ensure inspection readiness. Don’t miss her invaluable insights 👉 https://hubs.ly/Q02Hd58y0 #RBQMLive2024 #RBQM #ClinicalTrials #ClinicalResearch
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Have you heard? 🗣 Registration for RBQMLive 2024 is OPEN! 🗓️ Get ready to dive into the future of risk-based quality management with the industry’s best and brightest, all from the comfort of your home. Expect groundbreaking insights, networking, and innovation. Don’t miss your chance to be part of the revolution. Snag your spot now and leave the rest to us! https://hubs.ly/Q02FbnD20 #RBQMLive2024 #ClinicalTrials #RBQM
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🚀 Meet Intelligent Medical Coding from CluePoints! 👋 Say goodbye to tedious manual processes and say hello to slick automation powered by advanced Deep Learning. Our tool seamlessly integrates with existing systems to offer precise, AI-generated coding suggestions. Ready to revolutionize your clinical trials? https://hubs.ly/Q02Fbhs-0 #MedicalCoding #ClinicalTrials #ClinicalResearch
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Big news! Lotte Smets will be taking the virtual stage at RBQMLive 2024 in September to present “RBQM Industry Guidance Evolution – Adapting to Modernization.” These are insights that can make a real difference in your next clinical trial. Registration is OPEN! 👉 https://hubs.ly/Q02Gf68L0 #RBQMLive2024 #RBQM #ClinicalTrials #ClinicalResearch