Medicines and Medical Devices Regulatory Agency (MMRA) Эм,Эм, эмнэлгийн хэрэгслийн тухай хууль /Шинэчилсэн найруулга/ (Law of 5 June 2024, revised edition)
Эм, эмнэлгийн хэрэгслийн тухай хууль /Шинэчилсэн найруулга/ (Law of 5 June 2024, revised edition) is the official MOH identifier for “Law on Medicines and Medical Devices (revised edition)”. Эм, эмнэлгийн хэрэгслийн тухай хууль /Шинэчилсэн найруулга/ (Law of 5 June 2024, revised edition) is the official identifier MOH uses for this instrument.
- Instrument
- Эм,
- Full name
- Эм, эмнэлгийн хэрэгслийн тухай хууль /Шинэчилсэн найруулга/ (Law of 5 June 2024, revised edition)
- Category
- General
- Authority source
- Mongolian
- Readable HTML
- 61 articles · 1 language version
- Published
- 5 June 2024
- Effective
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Law on Medicines and Medical Devices (revised edition)
Эм, эмнэлгийн хэрэгсэл, эмийн тухай хууль, revised edition adopted at the State Palace, Ulaanbaatar on 5 June 2024 and in force from 1 October 2024 (Art. 61.1). Chapters 1–10 and Articles 1–61. The device regime sits in Chapter 4 (medical-device control and regulation), with Chapter 2 governing the special licences an operator must hold, Chapter 3 the medicines regime, Chapter 5 health supplements, Chapter 6 import and export, Chapter 7 procurement and price control, Chapter 8 the role of state bodies and non-state organisations, and Chapter 9 inspection. Art. 4.1.10 defines the medical device and its sub-terms (laboratory/IVD device, medical equipment, medical consumables). Adopted by the State Great Khural; the Ministry of Health is the administrative body the law charges with the register. The retrieved legalinfo.mn expression carries the legal database's own inline amendment notes to individual articles, including the law of 3 July 2026, and is ingested as the consolidated text the database serves.
Эм, эмнэлгийн хэрэгслийн тухай хууль /Шинэчилсэн найруулга/ (Law of 5 June 2024, revised edition) is the official identifier MOH uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.