eKare inSight
inSight is a comprehensive integrated suite of applications designed to empower researchers with accurate and timely information. The wound assessment and documentation are streamlined with single image capture and synced to a secure HIPAA, GDPR, and 21 CFR Part 11 compliant environment. Create a unified integrated research experience. Leverage emerging data and clinical evidence to develop study protocol, imaging charter, and adjudication manual. Build and configure the database with ease and efficiency. Customize clinical workflow and integrate seamlessly with your EDC. Dedicated project manager to ensure timely start and project maintenance. De-risk your clinical study with the highest quality standards, quality assurance, and control procedures. Analyze data and uncover insights in real time. Curate data sets, and augment clinical studies with real-world evidence. Our wound imaging solution is CE-marked and registered with the FDA. It has been clinically validated.
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Castor EDC
Castor is a leading platform for clinical data management, offering advanced solutions for electronic data capture (EDC), patient-reported outcomes (ePRO), and eConsent. Designed to streamline clinical trials, Castor enables researchers to efficiently collect and manage data from multiple sources in a compliant, user-friendly environment. The platform also supports decentralized trials (DCTs), providing tools for remote patient recruitment, monitoring, and real-time data analysis. Castor is trusted by over 50,000 users globally, helping clinical research teams accelerate trials while ensuring high-quality data and regulatory compliance.
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SAS Life Science Analytics Framework
Only SAS delivers a single, open, cloud-native statistical computing environment for clinical research with embedded analytic tools, support for data standards, and optional integrated analytic applications. Our analytic foundation for clinical research helps you modernize and deliver new therapies to market faster to improve health. Manage and analyze information in a collaborative platform, streamline processes, and more efficiently deliver trial results to regulatory authorities. Provides a cloud-native, single solution for clinical analysis and submission with everything you need for validation, regulatory compliance, versioning, audit trails, and documentation support. Allows for automation through workflows, support for current and future integrations, and implements and properly manages data standards and controlled terminology. Includes central hub for all incoming data, automated data quality analysis, better data management, and analytical data preparation.
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Signant Health
Signant Health is a global evidence-generation company that helps modernize clinical trials by meeting patients where they are and reimagining the path to proof. They offer comprehensive clinical technology solutions, including electronic Clinical Outcome Assessments (eCOA), Electronic Data Capture (EDC), electronic clinician ratings, and a unified eClinical platform. Their patient engagement tools encompass a patient engagement app, eConsent, and telemedicine capabilities. Signant Health also provides clinical data and analytics services, such as COA data analytics and data aggregation and intelligence. With over 30 years of experience, they have supported thousands of trials and contributed to hundreds of drug approvals, making them a trusted partner for sponsors and CROs aiming to deliver high-quality data for trial decisions and regulatory submissions.
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