Our platform provides a line of sight across your trial portfolio while eliminating the busy work that burdens most clin ops teams and falls through the cracks of other systems.
ClinOps Pro helps you steer your trials to the correct destination, with quality and speed. Access actionable insights to surface real-time risks, decision points, trends, and near-term deliverables. It can also surface lessons learned from prior trials to help you optimize future trials. Learn more.
Pharma sponsors: Gain autonomy and control by owning your trial portfolio data, reporting, and insights. Standardize your trial management and reporting despite variation in study teams, CROs, and vendors. Let your CRO focus more on detailed trial execution. Learn more.
CROs: Serve your pharma clients more efficiently, with less resources. Also delight them by proactively providing unique, actionable insights that differentiate your services. Learn more.
ClinOps Pro is an enterprise cloud platform that is HIPAA, 21 CFR Part 11, GDPR, and CCPA compliant. It is validated through the industry-standard GAMP-5 approach to Compliant GxP Computerized Systems. Our platform also has 99.9% uptime. We take your data accessibility, security and privacy seriously.
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As a trial progresses, the data needing oversight increases exponentially. Having to navigate to multiple clinical trial systems (or files) to gather trial data or insights results in numerous, inefficient workflows. These result in incomplete oversight and slower decisions. ClinOps Pro eliminates this problem. Learn more.