Enforcement record
Administrative Guidance disclosure naming 医薬局
This page records one action from a Japanese government disclosure, including the published name, governing law, authority, action details, and official source.
Action type
Administrative Guidance
Law
Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices
Authority
Ministry of Health, Labour and Welfare
Action date
Unknown
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-YI-YAO-JU-202607261653
- Generated at
- 27 July 2026 at 01:53
- Record URL
- https://regbase.jp/en/enforcement/yakkiho-yi-yao-ju-unknown
1. Review Summary
| Disclosure name | 医薬局 | Corporate Number | Not stated in the disclosure |
|---|---|---|---|
| Enforcement record | 1 record | Other confirmed records for this company | Outside this report's scope |
| Action date | Unknown | Authority | Ministry of Health, Labour and Welfare |
| Law | Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices | Action type | Administrative Guidance |
| 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 | 医薬局 |
|---|
3. Enforcement Record
| Target name in disclosure | 医薬局 |
|---|---|
| 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 / Administrative Guidance |
| Action / announcement date | Action: Unknown / Announcement: 10 April 2026 |
| English summary | Medical Devices and Living Hygiene Bureau, Medical Devices Review and Safety Management Division, 21st Regular Meeting on Approval Review and Safety Measures for Medical Devices and In Vitro Diagnostic Drugs |
| Original Japanese text | 医薬・生活衛生局 医療機器審査管理課 第21回医療機器・体外診断薬の承認審査や安全対策等に関する定期意見交換会 |
| Official source | https://www.mhlw.go.jp/stf/newpage_35771.html |
| Source archive | https://kiroku.today/a/7547e0e12ahgrl5k |
| Extraction / evidence timestamps | Extracted: 25 April 2026 at 09:21 / Evidence checked: 25 April 2026 at 09:21 / Archive captured: 12 July 2026 at 16:22 |
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 医薬局
Includes the published name, regulator, governing law, source links, archive status, and reviewer note fields for internal due-diligence files.
Preserved evidence by Kiroku
Review the preserved source for 医薬局
Open the preserved public source with its capture time, original artifact, available verification data, and downloadable evidence pack.
For developers: JSON integration details
You do not need this for normal browsing. Use it only when integrating this enforcement record into an internal tool or AI workflow.
Action summary
- Company
- 医薬局Japanese onlyOriginal: 医薬局
- Governing law
- Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices薬機法
- Action type
- Administrative Guidance行政指導
- Action date
- Unknown
- Issuing authority
- Ministry of Health, Labour and Welfare厚生労働省
- Industry context
- 医療機器規制
Violation
Medical Devices and Living Hygiene Bureau, Medical Devices Review and Safety Management Division, 21st Regular Meeting on Approval Review and Safety Measures for Medical Devices and In Vitro Diagnostic Drugs
Show original Japanese text
医薬・生活衛生局 医療機器審査管理課 第21回医療機器・体外診断薬の承認審査や安全対策等に関する定期意見交換会
Compliance context
Low-mediumAdministrative guidance or supervision was publicly disclosed by the authority.
Health product law covering pharmaceuticals, medical devices, cosmetics, quasi-drugs, labeling, and advertising.
Use as a monitoring signal. Confirm details before treating it as a formal sanction.
This context is an operational aid for review workflows, not a credit opinion or legal conclusion.
Evidence pack
- Extracted at
- 2026-04-25T00:21:39.604+00:00
- Evidence checked
- 2026-04-25T00:21:39.604+00:00
- Archive captured
- 2026-07-12T07:22:13.215214+00:00
Show audit JSON
{
"record": {
"id": "57a7de35-c715-4c11-8d32-51d6a4c66888",
"url": "https://regbase.jp/en/enforcement/yakkiho-yi-yao-ju-unknown",
"company_name_original": "医薬局",
"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": "行政指導",
"en": "Administrative Guidance"
},
"authority": {
"ja": "厚生労働省",
"en": "Ministry of Health, Labour and Welfare"
}
},
"entity_match": {
"status": "unresolved",
"confidence": 60,
"method": "linked_profile_without_source_identifier",
"method_label": "linked_profile_without_source_identifier",
"notes": "The linked profile has a Corporate Number, but the public disclosure does not contain that number and no unique independent NTA name/address match was found."
},
"review": {
"status": "unreviewed",
"label": "Machine extracted"
},
"compliance_context": {
"severity": "Low-medium",
"actionMeaning": "Administrative guidance or supervision was publicly disclosed by the authority.",
"practicalNote": "Use as a monitoring signal. Confirm details before treating it as a formal sanction.",
"lawContext": "Health product law covering pharmaceuticals, medical devices, cosmetics, quasi-drugs, labeling, and advertising."
},
"evidence": {
"recordUrl": "https://regbase.jp/en/enforcement/yakkiho-yi-yao-ju-unknown",
"officialSourceUrl": "https://www.mhlw.go.jp/stf/newpage_35771.html",
"officialDocumentUrl": null,
"archiveUrl": "https://kiroku.today/a/7547e0e12ahgrl5k",
"archivedSourceUrl": "https://www.mhlw.go.jp/stf/newpage_35771.html",
"archiveCapturedAt": "2026-07-12T07:22:13.215214+00:00",
"extractedAt": "2026-04-25T00:21:39.604+00:00",
"translatedAt": "2026-05-01T07:09:50.438+00:00",
"evidenceCheckedAt": "2026-04-25T00:21:39.604+00:00",
"generatedAt": "2026-07-26T16:53:59.341Z"
},
"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.