Russian Federation:
Procedure For The Issue Of Documents On Stages Of The Medicine Manuacturing Process In The EAEU Territory And On The Medicine Manufacturing Compliance With GMP
02 August 2016
GRATA International
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On 29 July 2016, the Orders of the Ministry of Industry and
Trade of the Russian Federation (Minpromtorg), dated 31 December
2015, entered into force that approved:
- the Administrative regulations for
the provision by Minpromtorg of the public service on the issue of
the document containing information on the stages of the medicine
manufacturing in the Eurasian Economic Union territory;
- the Administrative regulations for
the provision by Minpromtorg the public service on the issue of the
document which confirms that a medicine for medical use is
manufactured in accordance with the requirements of the good
manufacturing practice (GMP) and shall be submitted at the request
- of the competent authority of a country where the medicine is
imported to.
The content of this article is intended to provide a general
guide to the subject matter. Specialist advice should be sought
about your specific circumstances.
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