Manufacturing license
TICEBA possesses a manufacturing license within the meaning of § 20 b and § 20 c of the German Medicines Act (authorization for the treatment or processing, preservation, storage of tissue or tissue preparations) in accordance with the authoritative European directives.
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All described activities are carried out by TICEBA in accordance with the authoritative European and German instructions in compliance with Good Practice (GMP - Good Manufacturing Practice). Under these strict conditions, your stored skin cells can be used in the case of need as raw material for the manufacturing of an autologous (from the patient himself) medicine. |
