Now accepting early access requests

Japan's Drug Approval Data. Finally in English.

Search, analyze, and monitor PMDA review reports — structured, translated, and updated daily.

PMDA publishes 500+ drug approvals per year. Only ~300 have ever been translated to English.

400+
Drug Reports
18 Years
of Data
Updated
Daily
$84B
Market Coverage

The Problem

The world's 3rd largest pharmaceutical market is locked behind a language barrier

Japanese-Only PDFs

Critical review reports, approval documents, and regulatory data are published exclusively in Japanese as unstructured PDF files.

No Structured Data or API

No machine-readable format, no search API, no structured database. Teams spend hours manually extracting data from scattered documents.

Weeks of Waiting

Hiring consultants or translation firms means weeks of turnaround time and thousands of dollars for a single review report.

The Solution

PMDA data, structured and translated

PharmaLens transforms raw Japanese regulatory documents into an actionable English intelligence platform.

Structured English Database

Every approval translated and organized into searchable, structured records.

Daily Monitoring & Alerts

Get notified the moment new approvals or safety updates are published.

Search by Drug / Indication / Company

Find exactly what you need with powerful filters across all PMDA data.

Full Review Report Summaries

AI-generated English summaries of complete PMDA review reports.

app.pmdaintel.com/dashboard

Recent Drug Approvals

Search drugs...
Drug NameCompanyIndicationDateStatus
KeytrudaMSD K.K.Non-small cell lung cancer2026-03-15Translated
EnhertuDaiichi SankyoHER2+ breast cancer2026-03-12Translated
OpdivoOno PharmaceuticalGastric cancer2026-03-08In Progress
LeqembiEisaiAlzheimer's disease2026-02-28Translated

Pricing

Simple, transparent pricing

Choose the plan that fits your regulatory intelligence needs.

Starter

$299/mo

For individuals exploring the Japanese pharma market.

  • Search & browse drug database
  • 20 full reports per month
  • Basic search filters
  • Email support
Join Waitlist
Most Popular

Professional

$799/mo

For regulatory affairs teams that need comprehensive access.

  • Unlimited report access
  • Daily monitoring & alerts
  • Full API access
  • Advanced search & filters
  • Export to CSV / PDF
  • Priority email support
Join Waitlist

Enterprise

$1,500/mo

For organizations requiring full historical coverage.

  • Everything in Professional
  • Team accounts (up to 10 seats)
  • Full historical data (18+ years)
  • Custom integrations
  • Dedicated account manager
  • Priority support & SLA
Contact Sales

Get Early Access

Be the first to know when we launch. Early subscribers get 30% off their first year.

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