The Go-To CRO Resource For All Things RBQM

CluePoints harnesses cutting-edge innovations in advanced statistics and machine learning to create AI-powered solutions that go beyond traditional data points and algorithms. Our enterprise software revolutionizes trials for CROs, supporting superior data review for superior trial outcomes.

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CluePoints helps CROs proactively mitigate risk in clinical trials, ensuring compliance with ICH guidelines and the validity of data collected. When you partner with CluePoints, the leader in Risk-Based Quality Management (RBQM), you gain access to the advanced software, extensive scale, and R&D investments that drive unparalleled innovation at an accelerated pace, surpassing what other CROs achieve independently. We don’t just streamline processes; we enhance overall efficiency and profitability in clinical trial operations.

FEATURED GUIDE

The Ultimate Guide to Risk-Based Quality Management (RBQM)

Whether you’re part of a small or large company, with one-to-many projects in the pipeline, specializing in pharmaceuticals or medical devices, RBQM covers a broad range of quality management activities to ensure overall trial quality, data integrity, and patient rights and safety. Get a copy of our guide, which offers an expert insider’s perspective on RBQM’s evolution and strategies for implementation.

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FEATURED BLOG

The Bold Future of RBQM for CROs

In a world where complacency is the enemy of progress, CROs stand at a crossroads. Traditional approaches have their merits, but they’re no match for the transformative power of RBQM. It’s time to be bold, challenge the status quo, and redefine your future. Continue reading over on our blog…

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FEATURED VIDEO

Mitigate Trial Risk.
Ensure Data Validity.

Embrace RBQM to future-proof your operations, gain a competitive edge, and stay ahead with CluePoints as your trusted partner. Beyond software, we deliver training to maximize utilization, ensuring seamless RBQM implementation, process alignment, and efficient oversight.

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What Our Clients Are Saying

Senior Manager

"The CluePoints experience is great. CluePoints is a very flexible tool and provides more insights to data analysis.”

Associate Director, Clinical Monitoring Operations

“It’s rare to find a vendor that understands both the technology and the operational side - the CluePoints team knows it all!”

Senior Central Monitor, RBM, Data Monitoring & Management

“CluePoints is a beneficial tool for statistically analyzing the clinical data and identifying potential risks in the ongoing data so as to facilitate timely action by the study team.”

Senior Manager, Enterprise Systems

“The CluePoints implementation team was extremely responsive and helpful throughout our SSO configuration and integration. They made the process seamless and painless. If you’re looking for a partner who’ll walk you through each step while also leading the way and supporting you, look no further than CluePoints. You won’t be disappointed!”

Clinical Project Manager

“It’s not only the software that supports the whole RBM process; it’s also the collaboration given by the CluePoints team that supports the individual RBM process for us.”

Quality & Risk Management Lead

“Intuitive, multiple data exploration options in addition to KRIs, robust risk communication module.”

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It’s no surprise that the most enlightening moments unfold when we put your data into our platform for the first time. Experience it yourself—get a demo and see the impact.

About CluePoints

CluePoints is the premier provider of RBQM and data quality oversight software. We’re leveraging the potential of artificial intelligence using advanced statistics and machine learning 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 in all trials. Coupled with thought leadership and consulting expertise to aid pre-study risk assessment, identification of risk controls, and solution implementation, you now have everything you need to adhere to global regulatory guidance. 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.

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