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AI Compliance Engine for Government & Hospital Portals

Streamline Regulatory Review. Reduce Manual Burden. Increase Trust.

Our AI engine is purpose-built for government portals and hospital procurement systems, automating the way regulatory teams process and assess medical device submissions.

Instead of manually reviewing long, repetitive documents, our engine helps you:

  • Automatically extract key information from submitted files

  • Identify missing or non-compliant content based on local regulations

  • Flag potential risks or inconsistencies

  • Generate structured summaries and pre-approval recommendation drafts

By integrating into your existing review workflow, our AI engine acts as a smart assistant—cutting paperwork, reducing human error, and speeding up the approval cycle.

Built for regulators. Designed for real-world compliance. Trusted by hospitals and health agencies.

📄 Pending Contracts for Review

Government Agent Portal · Powered by AI-Driven Compliance Analysis

Effortlessly review incoming contracts and technical documents with real-time AI insights.
Our system highlights key sections, flags compliance risks, and accelerates decision-making—so you can focus on what truly matters.

🏭 Manufacturer: QingCare Medical Devices Ltd.

Product Applicant: Sterile Surgical Glove

  1. Import Licensing Agreement – Japan MAH Format (JP-IL-1043)

  2. EU Authorized Representative Contract (EU-REP-2119)

  3. Sterilization Compliance Declaration Form (SCDF-EU-JP-GLV)

  4. Product Labeling Attestation (JP/EU Format, Multi-language)

🏭 Manufacturer: VinaHealth Tech Co., Vietnam

Product Applicant: CO₂ Sampling Line (Disposable)

  1. EU Market Registration Notification Letter (EU-MDR-F12)

  2. Customs Pre-Approval Form for Class I Device (EU-IMF-341)

  3. Certificate Validation Agreement – CE to Local Use (EU-CVA-2023)

  4. Product Usage Traceability Protocol (P-UTP-EU-2024)

🏭 Manufacturer: SakuraMed Industrial Co.

Product Applicant: Oropharyngeal Airway (Soft Curve)

  1. Distribution Authorization Form – Japan (JP-DA-0903)

  2. GVP/GPSP Compliance Acknowledgment (JP-REG-442)

  3. Packaging Language Certification Agreement (JP-PLC-2023)

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