Medical devices are regulated by the Ministry of Health (MOH).
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.
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