Castor

Maintain full audit trails for every change to study data and configuration, ensuring regulatory readiness and inspection compliance

Framework to help with ICH E6(R3) compliance and functional oversight requirements

Manage study amendments in a secure, traceable, and validation-friendly environment with separate test environments to validate updates before deployment

Comply with FDA 21 CFR Part 11, ICH GCP, GDPR, HIPAA, ISO 27001, and ISO 9001 with support for HL7 FHIR and other clinical data standards

Oversee Source Data Verification status to ensure timely verification and regulatory readiness across study sites

Capture, process, and integrate clinical trial data from multiple sources and vendors on a compliant EDC system with centralized data management

Support direct electronic data capture in the field through eSource integration, connecting decentralized clinical trial components

Identify data gaps and delays early by monitoring outstanding queries and incomplete records across sites

Automatic query generation with easy response and data edit capabilities for efficient data review and validation

Reuse and clone eCRFs across studies to accelerate startup and ensure consistency across multiple trials

Deploy low-complexity clinical trials in as little as 3-4 weeks and reduce overall build times by up to 63%

Build advanced electronic case report forms in minutes with a low-code interface, enabling users to create custom eCRFs without extensive technical expertise

Manage data for the entire medical device and diagnostics development lifecycle and reduce time-to-market

Flexible, API-driven platform that integrates data from EHR, eCRF, ePRO/eCOA, laboratory systems, wearables, and other devices into a single clinical trial data environment

Support for studies in 20+ languages enabling global clinical trial execution

Capture and manage patient data through electronic patient-reported outcomes and clinical outcome assessments on a centralized platform, replacing paper surveys

Put patient diaries and surveys on a user-friendly mobile app that connects study participants from the comfort of their home

All-in-one solution to remotely recruit, screen and enroll patients with electronic informed consent and effortless patient experiences

Clinical trial participants are onboarded remotely via dedicated landing pages, prescreening, and video-enabled informed consent

Maintain >99.9% platform uptime and 100% data integrity for continuous clinical trial operations

Monitor clinical trial progress, data quality, and site performance in real time with live dashboards showing enrollment, data entry status, and key study metrics

Store clinical trial data securely with field-level encryption, two-factor authentication, real-time data saving, and long-term data retention on certified, compliant servers

Start with pre-built, validated eCRF templates designed for clinical trials and customize them using multiple field types and conditional logic

Integrated solution combining EDC, eConsent, ePRO, and API capabilities to support hybrid and decentralized trials in the era of COVID-19 and beyond

Build studies on your own with no training required, leveraging low-code tools and intuitive interface design