Import License

TICEBA possesses an import license in accordance with §72b, subsection 2, first sentence nr. 2 of the German Medicinal Products Act for both our tissue removal centers: Vitallife Corporation Ltd. in Bangkok, Thailand and the St. Luke's Medical Center in Manila, Philippines (authorization for the treatment or processing, preservation, storage of tissue or tissue preparations). Once received, all described activities are carried out by TICEBA in accordance with the authoritative European and German instructions in compliance with Good Manufacturing Practice (GMP).

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) or allogeneic (from a donor) medicine.

 

 

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License

Besides the authorization to manufacture a human medicinal product in accordance with § 13 (1) of the German Medicinal Products Act (AMG) for autologous mesenchymal stem cells, TICEBA is also authorized to manufacture a medicinal product for allogeneic mesenchymal as well as allogeneic limbal ABCB5 + stem cells following a recent extension. For more information click HERE.

Clinical Trial

Together with our subsidiary RHEACELL we are recruiting patients with the indication chronic venous ulcer (CVU) for the clinical trial in phase 1/2a. For more information click HERE.

The Story of Stem Cells

Review our category "The Story of Stem Cells" with the newest topic "Stem cells in wound healing" HERE.

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