Castor

About Castor

Castor provides a cloud-based clinical data platform that integrates electronic data capture (EDC), electronic patient-reported outcomes (ePRO), and electronic consent (eConsent) to facilitate decentralized clinical trials. This platform enables researchers to efficiently collect, manage, and analyze data from multiple sources while ensuring compliance with regulatory standards, ultimately reducing the time and complexity of clinical trial processes.

```xml <problem> Clinical trials often face challenges in efficiently capturing, managing, and integrating data from various sources, including electronic health records, patient-reported outcomes, and wearable devices. Traditional methods can be time-consuming, costly, and prone to errors, hindering the progress of research and development. Ensuring compliance with regulatory standards such as GDPR, HIPAA, and 21 CFR Part 11 adds further complexity. </problem> <solution> Castor provides a unified, cloud-based eClinical platform designed to streamline data capture and management for clinical trials. The platform integrates electronic data capture (EDC), electronic patient-reported outcomes (ePRO), and electronic consent (eConsent) modules to facilitate efficient data collection from multiple sources. By centralizing data management, Castor enables researchers to monitor study progress in real-time, improve data quality, and accelerate trial timelines. The platform's self-service capabilities and user-friendly interface empower researchers to build and deploy studies with minimal support, while ensuring data security and regulatory compliance. </solution> <features> - Integrated EDC, ePRO, and eConsent modules for comprehensive data capture - Compliant with 21 CFR Part 11, ICH e6 GCP, GDPR, and HIPAA regulations - Real-time reporting and monitoring of study health and progress - Secure data storage with ISO27001 and ISO9001 certifications - Patient-facing technology to remotely recruit, screen, and enroll patients - Integration capabilities with various data sources and vendors - Self-service platform for easy study building and deployment - Electronic data capture (EDC) system to maximize productivity by capturing, processing, and integrating data from multiple sources and vendors </features> <target_audience> The primary target audience includes researchers in biotech and pharmaceutical companies, medical device and diagnostics firms, contract research organizations (CROs), and academic institutions involved in clinical trials and real-world evidence studies. </target_audience> ```

What does Castor do?

Castor provides a cloud-based clinical data platform that integrates electronic data capture (EDC), electronic patient-reported outcomes (ePRO), and electronic consent (eConsent) to facilitate decentralized clinical trials. This platform enables researchers to efficiently collect, manage, and analyze data from multiple sources while ensuring compliance with regulatory standards, ultimately reducing the time and complexity of clinical trial processes.

Where is Castor located?

Castor is based in City of New York, United States.

When was Castor founded?

Castor was founded in 2011.

Location
City of New York, United States
Founded
2011
Employees
280 employees

Find Investable Startups and Competitors

Search thousands of startups using natural language

Castor

⚠️ AI-generated overview based on web search data – may contain errors, please verify information yourself! You can claim this account with your email domain to make edits.

Executive Summary

Castor provides a cloud-based clinical data platform that integrates electronic data capture (EDC), electronic patient-reported outcomes (ePRO), and electronic consent (eConsent) to facilitate decentralized clinical trials. This platform enables researchers to efficiently collect, manage, and analyze data from multiple sources while ensuring compliance with regulatory standards, ultimately reducing the time and complexity of clinical trial processes.

castoredc.com20K+
Founded 2011City of New York, United States

Funding

No funding information available.

Team (250+)

No team information available.

Company Description

Problem

Clinical trials often face challenges in efficiently capturing, managing, and integrating data from various sources, including electronic health records, patient-reported outcomes, and wearable devices. Traditional methods can be time-consuming, costly, and prone to errors, hindering the progress of research and development. Ensuring compliance with regulatory standards such as GDPR, HIPAA, and 21 CFR Part 11 adds further complexity.

Solution

Castor provides a unified, cloud-based eClinical platform designed to streamline data capture and management for clinical trials. The platform integrates electronic data capture (EDC), electronic patient-reported outcomes (ePRO), and electronic consent (eConsent) modules to facilitate efficient data collection from multiple sources. By centralizing data management, Castor enables researchers to monitor study progress in real-time, improve data quality, and accelerate trial timelines. The platform's self-service capabilities and user-friendly interface empower researchers to build and deploy studies with minimal support, while ensuring data security and regulatory compliance.

Features

Integrated EDC, ePRO, and eConsent modules for comprehensive data capture

Compliant with 21 CFR Part 11, ICH e6 GCP, GDPR, and HIPAA regulations

Real-time reporting and monitoring of study health and progress

Secure data storage with ISO27001 and ISO9001 certifications

Patient-facing technology to remotely recruit, screen, and enroll patients

Integration capabilities with various data sources and vendors

Self-service platform for easy study building and deployment

Electronic data capture (EDC) system to maximize productivity by capturing, processing, and integrating data from multiple sources and vendors

Target Audience

The primary target audience includes researchers in biotech and pharmaceutical companies, medical device and diagnostics firms, contract research organizations (CROs), and academic institutions involved in clinical trials and real-world evidence studies.

Want to add first party data to your startup here or get your entry removed? You can edit it yourself by logging in with your company domain.