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Allows for clinical-grade human embryonic stem cell line derivation and banking
August 20, 2018
By: Tim Wright
Editor-in-Chief, Contract Pharma
The Medical Products Agency (MPA), the Swedish national authority responsible for regulation and surveillance of the development, manufacturing and marketing of drug and other medical products, recently granted Takara Bio a manufacturing license for derivation and banking of human embryonic stem (hES) cells to be produced under GMP conditions at the state-of-the-art laboratory located in Göteborg, Sweden, within Takara Bio Europe’s facility. Since October 2014, Takara Bio has been offer...
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