Monitoring Intelligence
Real-time Regulatory Intelligence from source to decision.
Obsidian Monitoring Advisory continuously tracks 200+ government and regulatory sources across 30+ jurisdictions. Delivering actionable intelligence to compliance, legal, and strategy teams worldwide.
Latest official insights
Stay ahead of the latest regulatory developments in your industry with our plug-and-play monitoring platform, ready to deploy from day one.
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Why Obsidian Monitoring Advisory
Why leading organizations trust us for regulatory intelligence.
100% official sources
Every data point comes directly from government agencies and regulatory bodies. Zero third-party aggregators, zero noise.
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Real-time monitoring
Our infrastructure scans sources 24/7 and delivers updates as they are published, so you know before the market does.
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Expert-curated intelligence
Sectorial and regional specialists analyze, classify, and contextualize every regulatory change for immediate actionability.
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Industries we cover
From chemicals regulation to sustainable finance, our platform delivers deep, sector-specific monitoring so your team never misses a critical regulatory change.
Chemicals & PFAS
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This industry covers the production, use, and commercialization of chemical substances and advanced materials subject to strict environmental and health regulations. Continuous updates to REACH and the progressive restriction of PFAS (“forever chemicals”) create significant compliance risk, as changes in regulatory status can instantly impact product viability, supply chains, and inventory valuation across manufacturing, automotive, aerospace, and consumer goods sectors.
ESG & CSRD
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This vertical monitors the rapidly evolving landscape of corporate sustainability reporting and green finance. With the implementation of CSRD and global ESG standards, companies must track updates to reporting metrics, delegated acts, and green taxonomies to maintain market access, investor trust, and regulatory compliance across all corporate sectors.
Life Sciences
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Focused on the highly regulated healthcare sector, this industry tracks critical updates from global health agencies (FDA, EMA, Swissmedic). It covers market authorization, clinical trial regulations, and quality standards for pharmaceuticals and medical devices, where a single regulatory shift can determine product viability and global market access.
Monitoring 200+ official sources worldwide
