Republic of Tajikistan - MedStandard
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Republic of Tajikistan

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  • Regulatory Authority:

State Supervision Service of Health Care and Social Protection of the Republic of Tajikistan

 

Ministry of Health of the Republic of Tajikistan.

  • Certificate validity period:

5 years

  • Language of labeling and documentation:

Russian

  • Legislations:

Law of the Republic of Tajikistan dated 19 July 202, №1893 “On medicine, medical goods and pharmaceutical activity”

 

Health codex of the Republic of Tajikistan dated 30 May 2017, No.1413

 

Regulation of the Ministry of Health and Social Protection of Population of the Republic of Tajikistan dated 21 August 2015 No.736 “On Approval of the Procedure for State Registration of Medicines and Medical Products in the Republic of Tajikistan”

  • Registration period:

5–6 months

  • Authorized Representative:

not required

A brief algorithm for registration of medical devices in Tajikistan:

01
01

Collection of documents

02
02

Approval of the Application with the manufacturer

03
03

Finalizing the dossier, obtaining medical device samples and submission to the state authority

04
04

Primary examination

05
05

Examination of the registration dossier by the departments of preclinical and clinical expertise and the department of standardization

06
06

Receipt of the invoice for the examination and payment initiation

07
07

Receipt of the registration certificate template and coordination of the specified data

08
08

Entering the medical device into the State Register

09
09

Issuance of the registration certificate.

Final price and terms procedures will be calculated according to your request