Enforcement record
先駆け審査指定制度対象品目の募集 disclosure naming 日本新薬株式会社
This page records one action from a Japanese government disclosure, including the published name, governing law, authority, action details, and official source.
Action type
先駆け審査指定制度対象品目の募集
Law
Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices
Authority
Ministry of Health, Labour and Welfare
Action date
5 October 2017
RegBase evidence report
Japanese public-record enforcement check
Saveable record of the published action, regulator source, source status, and review notes for internal compliance files.
- Report ID
- RB-EN-ENFORCEMENT-YAKKIHO-RI-BEN-XI-202608041528
- Generated at
- 5 August 2026 at 00:28
- Record URL
- https://regbase.jp/en/enforcement/yakkiho-ri-ben-xin-yao-20171005
1. Review Summary
| Disclosure name | 日本新薬株式会社 | Corporate Number | Not stated in the disclosure |
|---|---|---|---|
| Enforcement record | 1 record | Other confirmed records for this company | Outside this report's scope |
| Action date | 5 October 2017 | Authority | Ministry of Health, Labour and Welfare |
| Law | Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices | Action type | 先駆け審査指定制度対象品目の募集 |
| Source status | Preserved public-source archive recorded | ||
This report summarizes public Japanese government disclosure data held by RegBase. It is not a credit score, sanctions conclusion, legal opinion, or adverse-media determination. Confirm important decisions against the linked official Japanese source.
2. Published Information
| Published name | 日本新薬株式会社 |
|---|
3. Enforcement Record
| Target name in disclosure | 日本新薬株式会社 |
|---|---|
| Authority | Ministry of Health, Labour and Welfare (厚生労働省) |
| Law / action type | Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices / 先駆け審査指定制度対象品目の募集 |
| Action / announcement date | Action: 5 October 2017 / Announcement: 27 April 2026 |
| English summary | The Ministry of Health, Labour and Welfare established the 'Designated Fast-Track Review System' on April 1, 2015, to promote the development of innovative pharmaceuticals, medical devices, regenerative medicine products, etc., with the aim of early practical application in Japan. |
| Original Japanese text | 厚生労働省は、革新的医薬品・医療機器・再生医療等製品を日本で早期に実用化することを目的として、その開発を促進するために、平成27年4月1日に「先駆け審査指定制度」を創設しました。 |
| Official source | https://www.mhlw.go.jp/stf/houdou/0000179802.html |
| Source archive | https://kiroku.today/a/ceb343f564hi8gdl |
| Extraction / evidence timestamps | Extracted: 28 April 2026 at 03:02 / Evidence checked: 28 April 2026 at 03:02 / Archive captured: 28 April 2026 at 03:03 |
4. Business Location and Permit Details
No additional structured business-location or permit fields are recorded for this disclosure.
5. Other Confirmed Records for This Company
This report covers the single government disclosure shown on this page.
Reviewer Notes
| Reviewer | Team / company | ||
|---|---|---|---|
| Review purpose | |||
| Additional notes | |||
- □ Official source URL or archived source was checked.
- □ Corporate Number, address, or other identifiers were reviewed to avoid confusing similarly named entities.
- □ This document is understood as a public-record evidence file, not a credit decision or legal opinion.
Current page: Enforcement record
This screen focuses on one disclosed action: the published name, governing law, authority, facts, source status, and review evidence.
Free report
Save the disclosure record naming 日本新薬株式会社
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Preserved evidence by Kiroku
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Open the preserved public source with its capture time, original artifact, available verification data, and downloadable evidence pack.
For developers: JSON integration details
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Action summary
- Company
- 日本新薬株式会社Japanese onlyOriginal: 日本新薬株式会社
- Governing law
- Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices薬機法
- Action type
- 先駆け審査指定制度対象品目の募集先駆け審査指定制度対象品目の募集
- Action date
- 5 October 2017
- Issuing authority
- Ministry of Health, Labour and Welfare厚生労働省
- Industry context
- 医薬品
Violation
The Ministry of Health, Labour and Welfare established the 'Designated Fast-Track Review System' on April 1, 2015, to promote the development of innovative pharmaceuticals, medical devices, regenerative medicine products, etc., with the aim of early practical application in Japan.
Show original Japanese text
厚生労働省は、革新的医薬品・医療機器・再生医療等製品を日本で早期に実用化することを目的として、その開発を促進するために、平成27年4月1日に「先駆け審査指定制度」を創設しました。
Compliance context
Context neededThis is a public Japanese regulatory disclosure. The exact legal effect depends on the cited source and regulator.
Health product law covering pharmaceuticals, medical devices, cosmetics, quasi-drugs, labeling, and advertising.
Review the original Japanese source and determine relevance to your counterparty-risk workflow.
This context is an operational aid for review workflows, not a credit opinion or legal conclusion.
Evidence pack
- Extracted at
- 2026-04-27T18:02:19.948+00:00
- Evidence checked
- 2026-04-27T18:02:19.948+00:00
- Archive captured
- 2026-04-27T18:03:15.938947+00:00
Show audit JSON
{
"record": {
"id": "ad1421eb-7c59-4b77-945f-59340be91e93",
"url": "https://regbase.jp/en/enforcement/yakkiho-ri-ben-xin-yao-20171005",
"company_name_original": "日本新薬株式会社",
"company_name_registry": null,
"corporate_number": null,
"law": {
"ja": "薬機法",
"en": "Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices"
},
"action_type": {
"ja": "先駆け審査指定制度対象品目の募集",
"en": "先駆け審査指定制度対象品目の募集"
},
"authority": {
"ja": "厚生労働省",
"en": "Ministry of Health, Labour and Welfare"
}
},
"entity_match": {
"status": "unresolved",
"confidence": 85,
"method": "nta_strict_name_nationally_unique",
"method_label": "nta_strict_name_nationally_unique",
"notes": "NTA full-download lookup found a nationally unique exact registered-name candidate (日本新薬株式会社). No Corporate Number was present in the disclosure, so this remains a likely match."
},
"review": {
"status": "unreviewed",
"label": "Machine extracted"
},
"compliance_context": {
"severity": "Context needed",
"actionMeaning": "This is a public Japanese regulatory disclosure. The exact legal effect depends on the cited source and regulator.",
"practicalNote": "Review the original Japanese source and determine relevance to your counterparty-risk workflow.",
"lawContext": "Health product law covering pharmaceuticals, medical devices, cosmetics, quasi-drugs, labeling, and advertising."
},
"evidence": {
"recordUrl": "https://regbase.jp/en/enforcement/yakkiho-ri-ben-xin-yao-20171005",
"officialSourceUrl": "https://www.mhlw.go.jp/stf/houdou/0000179802.html",
"officialDocumentUrl": null,
"archiveUrl": "https://kiroku.today/a/ceb343f564hi8gdl",
"archivedSourceUrl": "https://www.mhlw.go.jp/stf/houdou/0000179802.html",
"archiveCapturedAt": "2026-04-27T18:03:15.938947+00:00",
"extractedAt": "2026-04-27T18:02:19.948+00:00",
"translatedAt": "2026-05-01T09:43:23.181+00:00",
"evidenceCheckedAt": "2026-04-27T18:02:19.948+00:00",
"generatedAt": "2026-08-04T15:28:20.190Z"
},
"limitations": [
"RegBase aggregates public Japanese government disclosures and does not provide a credit opinion.",
"English summaries are provided for reference. The original Japanese source is authoritative.",
"Possible or unresolved entity matches should be manually verified before use in a decision."
]
}The original Japanese disclosure is the authoritative record. Use possible or unresolved matches only as leads for manual review.
Language
日本語版を見る (Japanese)About this recordAggregated and translated from public Japanese government disclosures. The English text is for reference only — authoritative content is the linked Japanese source.