Centralize. Collaborate. Comply. Accelerate Every Trial.

Independent Oversight Committees
with Cloud Concinnity

For Data Safety Monitoring Board, Data Monitoring Committees, and other safety review bodies

Simplify Your Oversight Activities From
DSMB and DMC to Other Independent Review Committees

At Cloud Concinnity®, we’ve developed an innovative platform to streamline and unify clinical trial workflows, with a focus on safety and oversight. Designed for high-level, cross-functional teams worldwide, we automate, orchestrate, and connect complex clinical business processes for seamless execution.

What's Slowing Down Your
Independent Committee Process?

If you’ve been stuck in endless spreadsheets, chasing down safety reports, or juggling disconnected tools, you're not alone. At Cloud Concinnity®, we’ve worked alongside clinical trial monitoring teams like yours. We've seen the same roadblocks, felt the same frustration, and built a smarter way forward.

No Real Time Safety Monitoring — No Real-Time Safety Monitoring

If you're manually tracking safety events and relying on manually executed tasks with limited visibility, you may be delaying adverse events (AE) & severe adverse events (SAE) reporting, putting your trial's quality at risk. When safety signals land in your inbox or slip through the cracks, the consequences can be serious.

Disconnected Safety Workflow

When your clinical trial communication isn't aligned across operations, pharmacovigilance, regulatory, and medical affairs teams, it shows. Siloed tools and poor document tracking can cause compliance problems and delays. Communication gaps make it worse.

Regulatory Compliance Gaps

Gaps between your electronic data capture (EDC) system and safety databases (50) can slow down SAE submissions and leave you exposed during inspections. Staying aligned with ICH E6 and global standards shouldn’t be this hard.

Safety Data All Over The Place — Safety Data All Over the Place

Managing clinical trial safety across global sites, vendors, and spreadsheets gets messy fast. Without standardized clinical workflow management, visibility drops, and your clinical trials oversight loses impact.

Your One-Stop
Safety & Compliance Hub

At Cloud Concinnity®, we have created clinical trial software that works the way your team does, so you can streamline your Independent Committee meeting scheduling, safety, and compliance from start to finish.

Effortlessly customize workflows to match your team’s specific needs with our intuitive no-code configurability. Designed for ease and flexibility, it ensures your clinical processes are streamlined and adaptable, saving time and enhancing efficiency across your team.
Stop chasing down forms and double-checking spreadsheets. We automate your safety submissions like DSURs, SUSARs, and PSURs. Our system includes regulatory templates and audit trails. You're always inspection-ready

No more delays. Our system auto-escalates AEs and SAEs, aligns with FDA, EMA, and ICH E2E standards, and assigns the right tasks using intelligent clinical trial dashboards and workflow management.
With Cloud Concinnity®, bring your CROs, Independent Committee, sponsors, and internal teams together on one platform. Boost decision-making with real-time and asynchronous collaboration, while dashboards, smart workflows, and a digital audit trail keep your trial running smoothly and your team always prepared.

Our platform fits your needs, whether it’s a single study or a global portfolio. Standardize your clinical workflows across geographies while maintaining visibility and control. With automated alerts and role-based access, your team stays aligned, informed, and always ready.

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