SureClinical

SureClinical is a cloud-based eClinical platform designed to streamline and expedite the management of clinical trials and regulatory processes. According to the vendor, SureClinical caters to companies of all sizes, ranging from small biotech startups to large pharmaceutical companies and healthcare organizations. It is utilized by professionals and industries such as Clinical Research Organizations (CROs), Pharmaceutical Companies, Biotechnology Companies, Medical Device Companies, and Healthcare Professionals to optimize their clinical trial operations and ensure adherence to industry standards.

Key Features

eTMF Management: SureClinical offers a comprehensive solution for securely creating, organizing, and managing trial-related documents, in compliance with regulations. Users can easily track document versions, classify and index documents, and manage their lifecycle.

Regulatory Document Management: SureClinical simplifies the management and tracking of regulatory documents throughout the submission process. It provides tools for document collaboration, review workflows, version control, and metadata management.

Clinical Operations Management: SureClinical streamlines and optimizes clinical trial operations with features such as study startup, site feasibility, document management, progress tracking, and data collection and analysis.

Document Collaboration and Sharing: SureClinical facilitates seamless collaboration and document sharing among study team members, sponsors, and other stakeholders. It ensures secure document sharing, change tracking, and access permissions management.

Audit Trail and Compliance: SureClinical ensures compliance with regulatory requirements by providing a robust audit trail that captures all document activities and changes. It enables tracking of revisions, access logs, and user actions for transparency and accountability.

Integration Capabilities: SureClinical supports integration with other clinical trial systems and tools, enabling seamless data exchange and interoperability with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and other third-party applications.

Document Workflow Automation: According to the vendor, SureClinical automates document workflows, reducing manual effort and improving efficiency. Users can create custom workflows for review and approval, ensuring timely completion of tasks.

Reporting and Analytics: SureClinical provides robust reporting and analytics capabilities to track and analyze key metrics related to document management, study progress, and compliance. It offers customizable dashboards, real-time data visualization, and advanced analytics tools.

Mobile Access: SureClinical offers mobile applications for convenient access and management of trial documents and data on the go. It supports offline access and data synchronization.

Data Security and Compliance: SureClinical prioritizes data security and compliance with industry standards and regulations. It implements data encryption, access controls, and conducts regular security audits to protect sensitive trial data.