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NOTICE

with regard to the manufacturing license:
TICEBA
possesses the required authorization by the competent authority for the manufacturing of tissue as source material of human origin for the manufacturing of pharmaceuticals in accordance with § 20 b and § 20 c of the German Medicines Act: Authorization for the treatment or processing, preservation, storage of tissue or tissue preparations.

Good Practice


For a few years already, TICEBA has been committed to compliance with the high standards in accordance with good practice.

gdpractice Any working procedure, manufacturing step and material is carried out by TICEBA in compliance with the high standards of Good Practice (GP). 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 both 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 clear written documentation of all steps in the process for the purpose of traceability.
Our production procedures are clearly defined and are followed by our staff strictly.
In order to guarantee the quality of the materials used as well as of the final product, we carry out strict quality controls at all times.

NEWS

TICEBA receives SME eligibility of EMA. continue »
TICEBA now on facebook. continue »
next event:
29. - 31. May 2012, ECOPRAM - European Congress on Preventive, Regenerative and Anti-Aging Medicine, Istanbul (Turkey). Topic: "Autologous pluripotent mesenchymal stem cells from the skin". Booth: 12. continue »

NEWSLETTER

INFORMATIONS

Request any information from us now.

COUNSELLING

"We are glad to counsel you in person", Dr. Christoph Ganss:
+49 (0)6221.718 33 0