Tajikistan
REGULATORY AUTHORITY: Medical devices are regulated by the Ministry of Health (MOH).

CLASSIFICATION SYSTEM:
Tajikistan follows the EU model of risk-based classification into Classes I, IIa, IIb and III.

TIMEFRAME: The registration process can range from three to six months, depending on the product type.

LICENSE VALIDITY: Licenses issued in Tajikistan are valid for five years.

AUTHORIZED REPRESENTATIVE: An authorized representative is required.

Last updated on January 10, 2018.



ARE YOU INTERESTED IN REGISTRATION IN TAJIKISTAN? REQUEST A FREE QUOTE>​

For ​ more information on registration in the Tajikistan, check out the following article on our blog:
Country at a Glance: Tajikistan
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