Good Manufacturing Practice (GMP)

For several years already, TICEBA has been committed to compliance with the high standards in accordance with Good Manufacturing Practice.

Any working procedure, manufacturing steps and material is carried out by TICEBA in compliance with the high standards of Good Manufacturing Practice. This is how TICEBA guarantees the best possible quality of your stem cells during preparation and storage.

Among others, our quality assurance contains the following points:

  • Our staff is highly qualified theoretically and practically, is trained regularly, and complies with the required hygiene standards.
  • Our premises and manufacturing equipment have been examined and meet the requirements of Good Practice.
  • We keep a clearly written documentation of all steps in the process for the purpose of traceability.
  • Our production procedures are clearly defined and are strictly followed by our staff.
  • In order to guarantee the quality of the materials used as well as of the final product, strict quality controls are carried out at all times.

Clinical Trials

We are now also recruiting patients for further clinical studies in phase I/IIa with allogeneic ABCB5-positive (ABCB5+) mesenchymal stem cells for the following indications: chronic venous ulcers (CVU), diabetic foot ulcers (DFU) and peripheral arterial occlusive disease (PAOD). For more information click HERE.


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.

The Story of Stem Cells

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