Logo
Sign in
Product Logo
Castor EDCCastor

Castor EDC simplifies clinical trial data capture and integration, offering a user-friendly platform with fast deployment and robust features.

Vendor

Vendor

Castor

Company Website

Company Website

Castors-CDMS-platform-enables-you-to-re-use-data-across-research-units.webp
1edf5ff84405fd29d44cb94e5598e917.webp
Deploy-your-study-faster-and-more-confidently.webp
Product details

Castor's electronic data capture (EDC) system streamlines the process of capturing trial data and seamlessly integrating it with other data within your clinical trial ecosystem. Ranked among the top 5% of EDCs for shortest build time, Castor enables the deployment of over 90% of studies within the first 4 weeks. The platform is designed with usability in mind, regardless of technical expertise, allowing users to build advanced eCRFs in minutes and navigate study complexities with best-in-class support. Castor facilitates better data flow by connecting and managing all trial components and integrations in one place, integrating data from EHR, eCRF, ePRO/eCOA, laboratory, wearables, and other devices through its open API. It also provides real-time visibility with a study health dashboard to monitor progress and outcomes, generate compliant data, and amend studies with less risk. Castor meets compliance certifications worldwide, such as FDA CFR Part 11, GDPR (EU), ICH GCP (HIPAA, US), ISO 27001, and ISO 9001, aligning with GCP, HL7 FHIR, and other regulatory guidelines.

Features:

  • Deploy studies faster: Castor is designed with usability in-mind for all, regardless of technical expertise.
  • Create better data flow: Connect and manage all trial components and integrations, in one place.
  • Gain real-time visibility: Monitor study progress and outcomes in real-time with Castor’s study health dashboard.
  • Generate compliant data, confidently: Build advanced eCRFs in minutes

Deploy studies faster Castor is designed with usability in-mind for all, regardless of technical expertise.

  • Build advanced eCRFs in minutes.
  • Deploy your study in as little as 4 weeks.
  • Navigate study complexities with best-in-class support.

Create better data flow Connect and manage all trial components and integrations, in one place.

  • Integrate data from EHR, eCRF, ePRO/eCOA, laboratory, wearables, and other devices.
  • Work with any software or database in your clinical trial ecosystem with Castor’s open API.

Gain real-time visibility Monitor study progress and outcomes in real-time with Castor’s study health dashboard.

  • Get an overview of study statistics as your studies are ongoing.
  • Track record data entry progress and outstanding queries.
  • View Verification Status (SDV) for Steps.

Generate compliant data, confidently Build advanced eCRFs in minutes

  • Start with one of our pre-built eCRF templates.
  • Customize your form with 21 different field types.
  • Clone and re-use forms as you build more studies.

Store data securely

  • Save study data in real-time.
  • Store it automatically on certified, compliant servers in any country.
  • Protect your data with 25-year data retention, field-level encryption, and two-factor authentication.

Amend studies with less risk

  • Simplify protocol amendments by using a tool that’s secure, trackable, and easy-to-validate.
  • Easily create test environments for each of your subsequent studies.

Achieve global compliance

  • Meet compliance certifications worldwide such as FDA CFR Part 11, GDPR (EU), ICH GCP (HIPAA, US), ISO 27001, and ISO 9001.
  • Align with GCP, HL7 FHIR, and other regulatory guidelines.