Medicines and Medical Devices Regulatory Agency (MMRA) АА/130 дугаар тушаал (Order A/130 of 6 June 2025)
А/130 дугаар тушаал (Order A/130 of 6 June 2025) is the official MOH identifier for “Procedure for Reporting, Recalling, Rapid Alerting and Destroying Medicines, Medical Devices and Health Supplements”. А/130 дугаар тушаал (Order A/130 of 6 June 2025) is the official identifier MOH uses for this instrument.
- Instrument
- А
- Full name
- А/130 дугаар тушаал (Order A/130 of 6 June 2025)
- Category
- Vigilance
- Authority source
- Mongolian
- Readable HTML
- 0 articles · 1 language version
- Published
- 6 June 2025
- Effective
- —
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Procedure for Reporting, Recalling, Rapid Alerting and Destroying Medicines, Medical Devices and Health Supplements
Эм, эмнэлгийн хяналт, зохицуулалтын газрын даргын 2025 оны 6 дугаар сарын 06-ны өдрийн А/130 дугаар тушаал, adopted under Art. 7.1.1 of the Law on the Legal Status of a Government Agency, Art. 40.1 of the General Administrative Law and Art. 50.2 of the Law on Medicines and Medical Devices. Four operative clauses: it approves, as Annex 1, the procedure for reporting, recalling, rapidly alerting and destroying medicines, medical devices and health supplements (clause 1); binds the heads of health and supply organisations and the directors of representative offices (clause 2); assigns the work to the Drug Safety Surveillance and Research Division and oversight to the Administration Division (clause 3); and repeals Order A/237 of 15 December 2022 (clause 4). Issued by the chairman of the Эм, эмнэлгийн хяналт, зохицуулалтын газар — the agency created by Government Resolution No. 222 — and signed in the chairman's temporary absence; the vigilance instrument that complements the registration procedure in Order A/206.
А/130 дугаар тушаал (Order A/130 of 6 June 2025) is the official identifier MOH uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.