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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.

Quality Management


The handling of human cells requires extreme diligence and the compliance with the highest safety standards. Due to our successful quality management, we are able to meet these requirements.


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Medicines Act

First and foremost, our product Back-up is subject to the Medicines Act. TICEBA holds the authorization for the manufacturing of tissue as source material of human origin for the manufacturing of pharmaceuticals in accordance with § 20b and § 20c of the German Medicines Act (AMG): Authorization for the treatment or processing, preservation, storage of tissue or tissue preparations. The application for the extension of the manufacturing license in accordance with § 20b and § 20c AMG for the enrichment of mesenchymal pluripotent stem cells out of autologous primary cell cultures has been submitted to the competent authorities at the end of July 2011.


Good Practice

Due to the high significance of "Good Practice" at TICEBA, this issue of quality management is contemplated separately.


Quality Assurance System

Tissue institutions are obligated by law and other requirements to set up a quality assurance system (QA-system). It is supposed to contribute to the proper proceeding of any procedures in connection with the manufacturing of the products. The required quality is thereby to be assured. In addition, a QA-system contributes to reaching a higher level of security with regard to complex proceedings; to enable employees to act on their own responsibility within the framework of clear specifications and to increase the trust of patients and employees in the institution.


TICEBA's quality assurance system consists of the following components:
Master documents contain a basic description of the quality concept and a description of premises and processes.
Standard operating procedures (SOPs) and operating instructions (AAW) exist for any quality-related process. SOPs describe superordinate processes, while AAWs regulate single processes and process steps in detail.
Implementation documents are protocols that are consulted by the employees on a daily basis in their professional day-to-day work.

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 »

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COUNSELLING

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