Centralize. Collaborate. Comply. Accelerate Every Trial.

Clinical Trial Oversight with
Cloud Concinnity

One intelligent platform for clinical trial oversight, process integration, and process automation,
centralizing your workflows, strengthening compliance, and accelerating decision-making

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Unify Your
Clinical Trial Process Management

Cloud Concinnity® seamlessly connects your clinical trial ecosystem, delivering end-to-end process integration and process automation. It simplifies how you organize information, collaborate with stakeholders, manage meetings, and document securely and compliantly, all within one secure, unified platform.

What’s Holding Your
Clinical Trials Back?

At Cloud Concinnity, we understand how challenging it is to navigate a fragmented clinical information management system. If you're relying on disconnected tools and outdated workflows, you're not alone, and we’re here to help you fix it so your teams can collaborate better & make faster, more confident decisions.

We See the Gaps in Your Clinical Trial Ecosystem

You’re switching between systems for clinical trial meeting scheduling, communication, and document tracking, and nothing feels truly connected
Your clinical management systems still rely on spreadsheets or email threads, making collaboration frustrating and error-prone
You lack the visibility to confidently support your Safety and Data Monitoring Committees or maintain real-time compliance monitoring

And Here’s What It’s Costing You

Your R&D costs are rising due to your clinical trial project management tools not working together
Your clinical trial workflows are delayed, hampering decision-making, pushing back key milestones, & slowing your pipeline
Gaps in regulatory compliance could lead to audit issues, lost trust, & funding challenges

Streamline Your
Clinical Information Management

An Automated Integrated Solution to Overcome Clinical Trial Complexities

Say goodbye to bottlenecks and blind spots. Cloud Concinnity® brings your entire clinical trial ecosystem together so you can move faster, stay compliant, and deliver results with confidence.

Improve Clinical Trial Access, Control & Information Security

Cloud Concinnity® ensures secure, role-based access to your clinical trial information. With a centralized document repository and integrated workflows, you prevent data leakage, simplify decision management, and maintain a single source of truth across your clinical trial ecosystem

Strengthen Compliance Monitoring & Risk Management

Our platform automates compliance with SOPs and regulatory standards, ensuring clinical trial oversight at every stage. Visual workflow tracking and secure information transitions reduce clinical trial risks and support regulatory readiness across the trial lifecycle

Accelerate Clinical Trial Efficiency & Workflow Automation

We turn your SOPs into automated workflows powered by process automation, cutting delays and boosting operational speed. With tools like live document editing, e-signatures, and automated meeting scheduling, you improve clinical trial timelines and drive higher clinical trial ROI

Enhance Clinical Trial Collaboration & Stakeholder Alignment

Improve collaboration across sponsors, CROs, and regulatory teams with real-time dashboards, KPI reporting, and seamless information sharing. Cloud Concinnity® delivers audit-ready transparency to support clinical trial governance

We help you Centralize your information, Collaborate your way, and Comply with confidence, so your team can focus on what truly matters.

Flexible Features, Personalized for
Your Clinical Workflow

Whether you're coordinating a global team, managing a data monitoring committee, or overseeing safety reviews, Cloud Concinnity® adapts to your unique workflows, streamlining clinical trial oversight with built-in process integration & automation.

With our cloud-based platform, we give you enterprise-grade security, two-factor authentication, and role-based access so only the right eyes see the right information at the right time
We make clinical trial reporting effortless. You get real-time dashboards, searchable audit trails, and eTMF-ready documentation, so your teams stay inspection-ready and aligned without chasing emails

With our flexible workflow engine, you can turn SOPs into automated processes, schedule DMC meetings, assign owners, and monitor milestones all in one place.
Edit documents in real-time, collect signatures with built-in 21 CFR Part 11 compliance, tag key stakeholders, and use our integrated dashboards, surveys, and meeting tools to drive smarter decisions across your clinical trial management