Seascape Clinical offers ClinOps Pro, a comprehensive clinical trial technology platform designed to enhance the efficiency and effectiveness of clinical operations. This platform automates and accelerates the clinical trial process, providing users with real-time visibility across their trial portfolios. ClinOps Pro enables sponsors, Contract Research Organizations (CROs), and Functional Service Providers (FSPs) to streamline their operations by eliminating redundant tasks and facilitating better communication among teams. The platform also offers actionable insights that help identify risks, trends, and deliverables, while leveraging lessons learned from previous trials to optimize future studies.

In addition to its operational benefits, ClinOps Pro prioritizes security and compliance, adhering to industry standards such as HIPAA, GDPR, and CCPA. The platform is validated through the GAMP-5 approach, ensuring it meets the necessary requirements for Good Automated Manufacturing Practice (GxP) computerized systems. With a commitment to data accessibility and privacy, ClinOps Pro boasts a 99.9% uptime, making it a reliable choice for organizations looking to improve their clinical trial management processes. Overall, Seascape Clinical's technology aims to empower pharma sponsors and CROs by providing them with greater control over their trial data and insights, ultimately leading to more efficient trial execution.

United States

Our Clinical Operations Oversight Solution ClinOps Pro, simplifies clinical trial oversight by consolidating inputs from all data sources and efficiently producing accurate, updated dashboards and trackers to facilitate critical decision making.

Seascape Clinical

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