Regulation Agency for Medical and Pharmaceutical Activities (RAMA) DocumentDocument No. 6157-Iს, 08/05/2012
Document No. 6157-Iს, 08/05/2012 is the official RAMA identifier for “Law of Georgia — Product Safety and Free Movement Code”. Document No. 6157-Iს, 08/05/2012 is the official identifier RAMA uses for this instrument.
- Instrument
- Document
- Full name
- Document No. 6157-Iს, 08/05/2012
- Category
- General
- Authority source
- English
- Readable HTML
- 146 articles · 1 language version
- Published
- 25 May 2012
- Effective
- —
- Consolidated through
- 2026-04-01
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Each version has stable article anchors for direct citations and highlighting. The readable text is generated from an authority source and does not replace the legally controlling publication.
Law of Georgia — Product Safety and Free Movement Code
Consolidated English text, current to 01/04/2026, of the Product Safety and Free Movement Code, Chapters I–X and Arts. 1–104. It is the general product-safety framework: responsibility for placing defective products on the market, general product-safety requirements, technical-threat control, technical regulations (Arts. 56–58 provide for their approval and for market surveillance), standardisation, traceability of measurements, conformity assessment, accreditation, and transitional and final provisions. The text names no medical device; it is the enabling framework under which the device technical regulations are approved, not a device-naming instrument.
Document No. 6157-Iს, 08/05/2012 is the official identifier RAMA uses for this instrument. Always confirm the current consolidated text and transition provisions with the official source before filing.