Public Consultation on revised Guideline for Registration of Medical Devices.

Bhutan Food and Drug Authority Version 1 original current

Imported from official source

The BFDA is sharing the guideline for your comments. This will be consulted for a period of two months from this share date. Your comments will be highly appreciated. The link for the Guideline is provided below: https://docs.google.com/document/d/1Xuxotqf2bk3ufeDdo98WSL_F70W9Y289/edit?usp=sharing&ouid=105735673346862547103&rtpof=true&sd=true

This version

Version
1 of 1
Recorded
October 03, 2026 20:42
Change
Initial
Content hash
09f08a58dd12fba2838628fd4d258dcb
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Officially records where a publication came from, not whether it is true. Imported records are reproduced from an organization's own official source.