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Pure Global AI Agents

Pure Global AI Agents is a free set of AI tools and open regulatory databases for medical device companies expanding into global markets. It covers device registrations, clinical trials, regulations, fees and timelines across dozens of countries, alongside AI agents for classification, documentation and translation work.

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Pure Global AI Agents screenshot
Pure Global AI Agents screenshot

Pure Global AI Agents (pureglobal.ai) is a MedTech-focused AI and open-data platform, distinct from Pure Global's separate regulatory-consulting service at pureglobal.com, which offers in-country representation, quality management and supplier audits. The AI agent platform's stated mission, quoted on its site from CTO Ran Chen, is "AI and open data as a force for global good," aiming to make medical device registration cheaper and faster rather than adding another paid SaaS layer. This description is grounded in an archived (Wayback Machine) snapshot of pureglobal.ai from May 2026, because the live site returned a rate-limited response at the time of this review; some details may have changed since.

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The core of the platform is a set of free, open databases: a global medical device database covering more than 1.9 million devices across more than 60 countries; a clinical trials database spanning more than 840,000 trials, 39 countries, 324,000+ diseases and 50,000+ sponsors; an official regulations library drawn from 5 sources across 10 categories; a registration timeline comparison tool across 29 countries and 4 risk levels; a government fee comparison tool across 25+ countries with live currency conversion to USD; and a directory of 25 regulatory consulting firms across 40+ countries. A country-by-country device database is also browsable by clicking individual countries on an interactive map, covering markets from Albania to Vietnam.

Alongside the databases sits an AI Agent Portfolio: a Regulatory Agent for real-time regulatory updates, compliance pathway recommendations and risk assessment; a Medical Device Registration Database agent for tracking regulatory status; a Medical Device Classification AI Agent for device classification and regulatory analysis; a Documentation Agent that automates document generation and review with multi-language support (stated as 20+ languages); and an AI Translation Agent specialized for MedTech terminology, covering 50+ language pairs. Additional tools listed include a company registry search across 6 countries, a regulation news feed (1,600+ updates from 18+ countries), a regulatory jobs board, a regulation FAQ library and step-by-step how-to guides.

Pure Global's site cites its own results: more than 500 clients served, more than 1,000 registration certificates obtained, and coverage of 30+ global markets, alongside claimed figures of 90% client retention, 95% approval success and 75% faster time-to-market. Named client quotes describe cutting FDA submission preparation time by 70%, entering 8 new European markets at once with a 300% revenue increase over 18 months, and catching a Japanese regulation change that a team had missed.

The core agents and databases are advertised as free; the site names Pricing as a separate section for anything beyond that, though no specific figures were visible in the material reviewed. The company lists an address in Jersey City, NJ, and names DJ Fang as a MedTech regulatory contact. Pure Global AI Agents is built for regulatory affairs teams and MedTech companies handling multi-country device registration, rather than for general compliance work outside the medical device space.

  • CategoryCompliance & Risk Management
  • Pricing ModelFlat Annual Fee
  • DeploymentCloud
  • PlatformsWeb

  • Free global medical device database covering 1.9M+ devices across 60+ countries

  • Free clinical trials database spanning 840K+ trials across 39 countries

  • Regulatory AI Agent for compliance pathway recommendations and risk assessment

  • Medical Device Classification AI Agent for global market classification

  • Documentation Agent that generates and reviews regulatory submissions with 20+ language support

  • AI Translation Agent for MedTech documents across 50+ language pairs

  • Registration timeline and government fee comparison tools across dozens of countries

  • Directory of 25 regulatory consulting firms across 40+ countries

  1. Open pureglobal.ai and pick a free tool: device database, clinical trials, regulations, timelines or fees.

  2. Search by country: select a country on the map or list to see its registration data.

  3. Try an AI agent: use the Regulatory Agent, Classification Agent or Documentation Agent for a specific device.

  4. Check the FAQ, or contact [email protected] for anything the free tools don't cover.

  5. Reach out to a specialist for markets that need paid registration support.

  • Regulatory affairs review
  • Early-stage market scoping
  • Regulatory documentation
  • Market access planning

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