CRIO

{
  "lawp_version": "0.3",
  "domain": "clinicalresearch.io",
  "name": "CRIO",
  "language": "en",
  "pages": {
    "/": {
      "title": "Intuitive eSource for Faster, Smarter Decisions | CRIO",
      "content": "The eSource solution that’s built for sites and better for your trials is clearly CRIO."
    },
    "/solutions/cros/": {
      "title": "CROs - Real-Time Remote Source Data Review to Increase Monitoring Productivity",
      "content": "The eSource solution for CROs seeking real-time remote source data review and measurably higher monitoring productivity. CRIO's Central eSource® gives CROs centralized oversight across all trial sites, live access to source data, and standardized templates - reducing monitoring burden and improving "
    },
    "/solutions/sites/": {
      "title": "Sites - Integrated eSource and CTMS to Streamline Operations and Data Capture",
      "content": "CRIO's integrated eSource and CTMS platform for clinical research sites streamlines operations, enables real-time source data capture, and supports remote monitoring. Purpose-built to reduce administrative burden, improve trial performance, and satisfy sponsor data quality requirements. Clearly CRIO"
    },
    "/products/esource/": {
      "title": "eSource - Real-Time Source Data Capture With Centralized Template Publishing and Remote Monitoring",
      "content": "CRIO's eSource platform enables clinical research sites to collect source data in real time and supports remote monitoring for sponsors and CROs. Offers centralized template publishing and real-time visibility across multicenter trials. Includes Central eSource® for sponsor-/CRO-led studies and Site"
    },
    "/products/site-ctms/": {
      "title": "Site CTMS - The Integrated eSource and CTMS Platform for Clinical Research Sites",
      "content": "CRIO's Site CTMS is a fully integrated eSource and CTMS platform for clinical research sites, combining patient scheduling, regulatory management, financial tracking, and real-time source data collection in a single system. Built to streamline operations and reduce administrative burden from study s"
    },
    "/solutions/sponsors/": {
      "title": "Sponsors - Implement Central eSource® to Boost Enrollment, Integrate With EDC, and Enable Remote Monitoring",
      "content": "How CRIO helps sponsors implement Central eSource® to boost enrollment rates and patient diversity across trial sites, integrate with existing EDC systems, streamline remote data review, and automate protocol-driven data capture - with demonstrated results of 40% faster startup and 90% gains in moni"
    },
    "/products/eregulatory/": {
      "title": "eRegulatory - Audit-Ready Digital Regulatory Binder for Clinical Research Sites",
      "content": "CRIO's eRegulatory solution manages regulatory documents, study files, and compliance workflows electronically. Supports FDA 21 CFR Part 11 compliance, inspection readiness, and audit-ready documentation for clinical research sites and site networks."
    },
    "/solutions/site-networks/": {
      "title": "Site Networks - Scalable eSource and CTMS for Clinical Trial Site Networks",
      "content": "CRIO supports site networks with scalable eSource and CTMS solutions that standardize data capture across all member sites, improve trial performance, and give network leadership centralized visibility into site operations and data quality."
    },
    "/products/esource/econsent/": {
      "title": "eConsent - Digital Informed Consent to Simplify Enrollment and Support Remote Trials",
      "content": "CRIO's eConsent digitizes the informed consent process for clinical trial participants, streamlining enrollment, improving participant diversity, and supporting remote and decentralized clinical trial workflows."
    },
    "/products/esource/site-esource/": {
      "title": "Site eSource - Electronic Source Data Capture Built for Clinical Research Sites",
      "content": "CRIO Site eSource is the purpose-built eSource solution for clinical research sites to capture source data electronically at the point of care. The only eSource system designed for sites by a site, with features honed over years of user feedback. Reduces manual transcription, supports real-time data"
    },
    "/products/esource/central-esource/": {
      "title": "Central eSource® - Improve Clinical Trial Site Performance and Reduce Protocol Deviations",
      "content": "CRIO's Central eSource® is the leading centralized eSource platform for improving clinical trial site performance and data quality. It centralizes template publishing to all sites and automates data flow into the EDC at scale, providing real-time visibility into source data, enabling remote source d"
    }
  },
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        "required": true
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      "intent": [
        "search",
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      "description": "Search CRIO"
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      "id": "book",
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      "name": "Shop products",
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      "description": "Get in touch with the site owner"
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      "name": "Subscribe",
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      },
      "intent": [
        "subscribe",
        "newsletter",
        "updates"
      ],
      "description": "Subscribe to the newsletter or updates"
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      "name": "Call",
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      "intent": [
        "call",
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        "telephone"
      ],
      "description": "Call 6173029845"
    }
  ]
}