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Signal detail view showing metadata, related products, and actions

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What you can do

  • Understand what changed and who issued it.
  • See which products might be impacted and why.
  • Save/share the signal and open the original source.

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Signal metadata

Each detail view consolidates essential intelligence parameters:
  • Source and Authority: Identifies the issuing body (e.g., World Health Organization) and the jurisdiction (e.g., Switzerland).
  • Impact and Sentiment Assessment: Provides a categorized impact rating (e.g., Medium Impact) and a sentiment analysis (e.g., Positive) to help users prioritize the urgency of the update.
  • Chronological Tracking: Displays the precise publication date and time to ensure the intelligence is current.
The “Related Products” section is the core analytical component of the details panel. It maps the regulatory signal to relevant medical devices within your inventory:
  • Automated Impact Logic: The system identifies products potentially affected by the regulatory change (e.g., AnesThesia X9, SleepWell Monitor).
  • Contextual Rationale: For every correlated product, the system provides a specific justification for the “Potential Impact.” For example, it may highlight how a new pandemic agreement could increase demand for specific workstations or how pathogen-sharing requirements might affect in-vitro diagnostic development.
  • Direct Product Navigation: Each product entry includes a hyperlink to the internal product master data, allowing for immediate cross-referencing of technical specifications and existing registrations.

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Actions

To facilitate rapid decision-making and data portability, the interface includes the following tools:
  • Ask AI: Initiates a natural language interaction with the AI assistant to summarize the signal, translate complex regulatory text, or extract specific action items.
  • Save and Archive: Allows users to bookmark critical signals for future reference or inclusion in periodic regulatory reports.
  • View Original: Provides a direct link to the official source document or the primary regulatory announcement to ensure data transparency and facilitate further legal or technical review.

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Tip

Use Ask AI to extract a short action list (who should review, what products to check, and what deadlines might apply), then validate against the source link.