Clincove

Accelerating Clinical Trials with Intelligence, Precision, and Trust

At Clincove, we’re on a mission to transform how clinical trials are run—making them faster, smarter, and more accessible for sponsors, sites, and patients alike.

We built Clincove to eliminate the operational bottlenecks that delay innovation.

With our unified platform, sponsors can manage medical records, automate eligibility decisions, streamline documentation, and gain real-time insights vall in one place. From Phase I to Phase III, Clincove empowers teams to move with clarity and confidence.

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Trial Protocols

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Investigator Documents

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Site Reports

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Site Initiation

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Monitoring Reports

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Regulatory Compliance

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Adverse Events

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Regulatory Submissions

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Ethics Committee Approvals

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Patient Records

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Study Completion Documents

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Clinical research is complex but managing it shouldn’t be.

Clincove was founded to simplify clinical operations through intelligent tools that reduce manual effort, improve compliance, and increase enrollment speed.

We believe in removing friction from trials so that the focus can stay where it belongs: on advancing health outcomes and getting therapies to the people who need them most.

Our Proven Impact

31% Faster Trial Completion compared to legacy systems

77% Reduction in Eligibility Review Time

HIPAA, 21 CFR Part 11, and GDPR compliant

Trusted across multiple therapeutic areas and trial phases

Our Values

Clarity over complexity: We design with the user in mind.

Speed with precision: Faster doesn’t mean sloppier—it means smarter.

Partnership-first: We don’t just provide software—we collaborate.