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.
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