Organizations united in advancing connected oversight, compliant AI adoption, and confident, inspection-ready execution.
Organizations united in advancing connected oversight, compliant AI adoption, and confident, inspection-ready execution.
Aligning risk-based oversight with global compliance expectations — including ICH E6(R3) inspection readiness.
Healthcare-AI certified MyRBQM® on Azure delivers secure, scalable oversight workflows that inspectors can trust.
Blending predictive analytics with expert QA to sharpen inspection confidence in complex trials.
Ergomed’s RBQM approach represents the future of clinical trial management.
Helping MedTech & biotech operationalize RBQM consistently and efficiently.
Tech Observer CRO delivers end-to-end services that drive the success of clinical trials at every phase.
Our EU R&D base supporting continuous RBQM product advancement and rapid prototyping.
Ergomed’s risk-based approach to quality management systematically identifies, assesses, and mitigates risks in clinical trials.
Blending predictive analytics with expert QA to sharpen inspection confidence in complex trials.
Tech Observer CRO provides valuable, real-time insights to help you stay ahead in a rapidly evolving market.
Our EU R&D base supporting continuous RBQM product advancement and rapid prototyping.
Healthcare-AI certified MyRBQM® on Azure delivers secure, scalable oversight workflows that inspectors can trust.
MongoDB Atlas speeds clinical insights with flexible data workflows powering our AI-augmented oversight. (See case study.)
Alementiv GI CRO has long-standing collaborations with partners who provide it with excellent local knowledge and expertise.
The Forschungsdock CRO GmbH company is a contract research organization (CRO) based close to the city of Hamburg.
Joint QTL methodology advancing data-driven tolerance-limit setting. (Publication expected Q1 2026.)
Validating trustworthy AI for clinical-grade signal detection and medical decision support.
Advancing clinical-trial AI with independent method validation under the LOEWE “AI-TRIAL” initiative.
Clinical-science expertise supporting AI that is safe, fair, and clinically interpretable.
Our EU R&D base supporting continuous RBQM product advancement and rapid prototyping.
Adamas and Cyntegrity help sponsors focus QA where it matters most — using centralized analytics to proactively detect risk signals and sharpen inspection confidence in complex oncology and rare-disease trials.
CROs, sponsors, research institutions, and regulators working together to execute RBQM in practice.
Expert Working Group
Shared learning to improve how RBQM is planned, executed, and evaluated in practice.
Oversight That Works
Developing practical tools — like reflective questions and oversight level guidance — that help teams confirm RBQM is delivering true value.
Led by Practitioners
Guided by Keith Dorricott, facilitated by Cyntegrity — turning shared challenges into actionable oversight progress.
Collaborate with us to bring safer, smarter clinical decision-making to life — through connected oversight, compliant AI, and scalable delivery. Together, we strengthen RBQM where it matters most.
These pages help you attract talent that aligns with your mission and mindset. They actively show that people want to work with Cyntegrity — and even more, work for your team. Additionally, they give enterprise clients clear confidence that your organization lives modern values such as ESG, ethics, and diversity. By combining culture, purpose, and responsibility, these pages create a strong first impression and guide visitors toward meaningful engagement.
The INDUSTRY SOLUTIONS page builds trust by directly addressing regulatory expectations and reducing perceived risk. It guides project, program, and operations leaders — as well as QA leads, regulatory officers, clinical compliance managers, and procurement teams — toward confident decisions. Moreover, the page clearly explains how your approach strengthens oversight and eliminates uncertainty, which helps these stakeholders move forward without hesitation.
These pages help you attract talent that aligns with your mission and mindset. They actively show that people want to work with Cyntegrity — and even more, work for your team. Additionally, they give enterprise clients clear confidence that your organization lives modern values such as ESG, ethics, and diversity. By combining culture, purpose, and responsibility, these pages create a strong first impression and guide visitors toward meaningful engagement.
The INDUSTRY SOLUTIONS page builds trust by directly addressing regulatory expectations and reducing perceived risk. It guides project, program, and operations leaders — as well as QA leads, regulatory officers, clinical compliance managers, and procurement teams — toward confident decisions. Moreover, the page clearly explains how your approach strengthens oversight and eliminates uncertainty, which helps these stakeholders move forward without hesitation.
These pages help you attract talent that aligns with your mission and mindset. They actively show that people want to work with Cyntegrity — and even more, work for your team. Additionally, they give enterprise clients clear confidence that your organization lives modern values such as ESG, ethics, and diversity. By combining culture, purpose, and responsibility, these pages create a strong first impression and guide visitors toward meaningful engagement.
The INDUSTRY SOLUTIONS page builds trust by directly addressing regulatory expectations and reducing perceived risk. It guides project, program, and operations leaders — as well as QA leads, regulatory officers, clinical compliance managers, and procurement teams — toward confident decisions. Moreover, the page clearly explains how your approach strengthens oversight and eliminates uncertainty, which helps these stakeholders move forward without hesitation.
The Trusted Compliance page strengthens regulatory confidence and helps decision-makers remove perceived risk. It speaks directly to QA leads, regulatory officers, clinical compliance managers, and procurement teams. Furthermore, the page demonstrates how your approach improves transparency, clarifies accountability, and supports consistent oversight. As a result, teams gain the reassurance they need to choose your solutions with conviction.
Key Capabilities pages introduce your technical and operational strengths without overwhelming visitors. They show how your system works, highlight real interoperability, and guide users toward requesting deeper technical information when they’re ready. Additionally, these pages maintain a teaser-first flow that encourages engagement and increases CTA actions rather than drowning readers in excessive detail. This balance helps prospects stay curious, confident, and eager to learn more.
The Connect & Deploy pages speak directly to clinical data leads, IT and integration specialists, and operational leaders evaluating compatibility. They demonstrate technical readiness, show how the platform connects with existing systems, and explain key integration flows. At the same time, these pages still follow your teaser-first, CTA-driven approach. Instead of overwhelming visitors with docs or schemas, they encourage teams to request the specific technical details they need, which strengthens engagement and supports a more personalized sales process.
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