Archive ready

「先駆け審査指定制度」に基づき、医療機器(3品目)、体外診断用医薬品(1品目)及び再生医療等製品(3品目)を指定 |報道発表資料|厚生労働省

https://www.mhlw.go.jp/stf/houdou/0000153128.html
April 7, 2026 at 09:02 PM JSTThe archive page, viewer, and downloads use this saved version.
April 7, 2026 at 09:02 PM JST·www.mhlw.go.jp

Bundle the HTML, screenshot, summaries, and metadata into one ZIP file. The first export request adds an external RFC 3161 timestamp before download.

Saved page

「先駆け審査指定制度」に基づき、医療機器(3品目)、体外診断用医薬品(1品目)及び再生医療等製品(3品目)を指定 |報道発表資料|厚生労働省

Open the dedicated viewer to inspect the saved page with archive metadata pinned above it.

StartedApril 7, 2026 at 09:02 PM JST

This is a self-contained HTML copy with CSS and images embedded, so it still renders even if the original page disappears.

The dedicated viewer keeps the original URL and saved timestamp visible while you review the archived HTML.

About this pageAI generated

This page is a press release from the Ministry of Health, Labour and Welfare dated February 28, 2017, announcing seven products designated under the "Pioneering Review Designation System." These include three medical devices, one in vitro diagnostic product, and three regenerative medicine products. The system aims to enable early practical application of innovative products in Japan, reducing the standard review period from 12 months to 6 months. Designated products include those developed from university research and by domestic SMEs and venture companies, expected to promote innovation and economic growth.

「先駆け審査指定制度」に基づき、医療機器(3品目)、体外診断用医薬品(1品目)及び再生医療等製品(3品目)を指定 |報道発表資料|厚生労働省 - Saved screenshot

The full page can be captured up to 15,000px in height so you can review the complete page layout when needed.