This milestone has been achieved on behalf of the Company by the NZPR Group who is the commercialisation partner of BLIS Technologies in China. The approval of BLIS K12 by the Chinese State Food and Drug Administration represents the end of a regulatory approval process that started in 2008.
This Chinese regulatory approval will enable NZPR Group to actively market BLIS K12 lozenges and associated BLIS K12 products through its distribution networks within the country. BLIS Technologies is extremely pleased with this achievement and anticipates it will soon be assisting NZPR Group further, with sales and marketing in China.
BLIS Technologies will enter into a market development partnership with Integra Medical, headquartered in Ontario Canada. Integra Medical will produce and sell retail products in the Eastern European market. Integra Medical has already successfully achieved regulatory approval for its first BLIS K12 based product as a dietary supplement within the Russian market and has now embarked upon several clinical trials to support its application for BLIS K12 based products as an approved medicine in Russia.
Source: BLIS Technologies
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