Japan — Pharmaceuticals and Medical Devices Agency
Tracked across 5 events · 34 articles · First seen May 12, 2026 · Last active Aug 05, 2026
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Regulatory
Impact: The PMDA is the regulatory authority reviewing Natera's application. Its decision will determine market access for Signatera in MIBC in Japan.
Aug 05, 2026 · 7 articles
Tech
Impact: The BD BACTEC FXI Culture System was licensed by the Japan — Pharmaceuticals and Medical Devices Agency for availability in Japan.
Jun 03, 2026 · 8 articles
Business
Impact: One of the acquired facilities underwent a Japan — Pharmaceuticals and Medical Devices Agency review in 2025 with clean results, demonstrating international regulatory compliance.
Jul 02, 2026 · 7 articles
Business
Impact: Japan's regulatory agency stated most new drugs require Japanese patient data, not solely Chinese studies.
Jul 15, 2026 · 6 articles
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