Entvin

Standardised, versioned global drug-label and product-authorisation corpus exposed as a REST API: approved product information normalised across 20+ regulatory authorities (US FDA, EMA, Health Canada, TGA, UK MHRA, Swissmedic, PMDA, SAHPRA, BfArM), sectioned into structured fields (product information, contraindications, adverse reactions, warnings and precautions), with retained version history, side-by-side cross-geography label comparison, approval-status and marketing-authorisation-holder attributes, and a change-event stream powering new-molecule-launch and label-update notifications.

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Sample

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Coverage

Universe, instruments and categories.

Industry: Financial Exchanges & DataPharmaceuticals
Instruments: equities
Categories: Reference

Dataset card

Type: not stated
Format: Multimodal leaning structured text — RESTful JSON API with Python and Node SDKs, plus long-form regulated label text in normalised sections with version lineage
Volume: est. high hundreds of thousands of product-label documents — 20+ authorities each publishing their own approved-product-information set, every document retained across multiple versions, so version lineage multiplies a six-figure base document count into a larger versioned record set
Users: N/A — API infrastructure product sold on keys and subscriptions rather than registered user accounts; request further research on customer count
History: 4 years
Update frequency: not stated
Growth: Active — sample records carry an April 2025 update stamp and the agency coverage is described as continuously expanding beyond the initial 20+ authorities
Launched: 2022 (company record marks the firm as a Y Combinator S22 batch company, and the API sample data carries 2025 update stamps)
Delivery: not stated
Entity mapping: not stated
Sample: not stated
Point-in-time: not stated
Licence: not stated

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