The Crosswalk
    NewPer-page social previews and this changelog

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    Changelog

    What changed on the Crosswalk and when. Subscribe with RSS to catch every regulator refresh.

    Last updated ·
    RSS feed8 entries · updated 2026-07-25
    1. Feature

      Per-page social previews and this changelog

      Every jurisdiction, pair comparison, and control checklist now renders its own Open Graph preview image, so links shared on LinkedIn and Slack show the actual page title and stats. This changelog and an RSS feed at /rss.xml track updates going forward.

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    2. UpdateComparison

      Cybersecurity depth pass across all 16 mapped jurisdictions

      Added a 'defaultEvidence' line to every one of the 24 existing control dimensions and appended five new ones: SBOM format/VEX cadence, recognized standards, cryptographic regime, vulnerability-disclosure clock, and AI/ML-specific expectations. Surfaced in the matrix tooltips, the pair checklist, and the CSV export.

      See it in the app
    3. Feature

      Start-here onboarding, persistent context bar, shareable planner

      Three-question guided router on the homepage seeds a saved context (target markets, risk class, intent) that persists across visits. The Planner now round-trips its full state through the URL so you can share a roadmap link with a colleague.

      See it in the app
    4. Regulator

      Taiwan TFDA, Thai FDA, and SAHPRA (South Africa) added

      Three new jurisdiction profiles: Taiwan (TFDA), Thailand (Thai FDA), and South Africa (SAHPRA), each with pre-market, SBOM, CVD, post-market, and penalties mapped against the FDA baseline. Also refreshed EU CRA timelines, UK MHRA CE-recognition posture, and Korea's Digital Medical Products Act.

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    5. FeatureComparison

      Pair checklist pages with per-row regulatory citations

      New /compare/checklist/:a/:b route shows a control-by-control side-by-side against the FDA baseline with a 'differences only' toggle, deep-link back into each playbook, and a CSV export. Every matrix row now carries a citation chip linking to the exact FDA/EU/UK/Korea section used to populate it.

      See it in the app
    6. UpdateGuidance

      Per-jurisdiction 'How to submit' playbooks

      Long-form submission playbooks on every standard page: how to submit, evidence checklist, common rejections, and typical timeline. HowTo JSON-LD is emitted per jurisdiction for search.

      See it in the app
    7. Feature

      Diligence ranking and Innovator Journey Planner

      New /planner wizard sequences a multi-market submission plan using a transparent multi-factor fit score. The Compare page adds a diligence ranking tab computing a 0-100 rigor score per jurisdiction with a factor-by-factor breakdown.

      See it in the app
    8. GuidanceRegulator

      FDA Feb 3, 2026 final guidance parsed into the FDA profile

      Updated the FDA entry to reflect the revised final guidance 'Quality Management System Considerations and Content of Premarket Submissions for Devices with Cybersecurity' (Feb 3, 2026), which supersedes the June 2025 version. Aligned with QMSR (21 CFR Part 820 / ISO 13485:2016).

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