doc. MUDr. Barbora Weinbergerová, Ph.D.
odborný konzultant
Our team investigates fundamental mechanisms and translates findings from bench to bedside, combining preclinical models with clinical insight.
Researcher at ICRC with focus on translational medicine. Combines preclinical insights with clinical practice across cardiology, neurology, and oncology programs.
Currently leads / contributes to interdisciplinary projects bridging molecular biology, imaging, and patient care at St. Anne's University Hospital Brno.
doc. MUDr. Barbora Weinbergerová, Ph.D.
odborný konzultant
Mgr. Jindřich Beránek
Lab Manager
Ing. Petra Česnek, Ph.D.
Lab Manager
RNDr. Daniela Hulínová
Production Manager
Mgr. Barbora Frimlová
Laboratory Technician Specialist
Mgr. Katarína Streďanská
Laboratory Technician Specialist
Mgr. Milan Hluchý, Ph.D.
Laboratory Technician Specialist
Mgr. Anna Macečková Brymová, Ph.D.
Laboratory Technician Specialist
Ing. Lucie Toufarová, Ph.D.
Laboratory Technician Specialist
Mgr. Eva Vaňharová
Laboratory Technician Specialist
RNDr. Lucie Kulišťáková
Laboratory Technician Specialist
Ing. Marie Vávrová
Kvalifikovaná osoba
Ing. Jana Šplíchalová, Ph.D.
Kvalifikovaná osoba
Mgr. Tereza Souralová, Ph.D.
Implementation Science Manager
doc. RNDr. Irena Koutná, Ph.D.
Head of CTEF
Mgr. Ivana Ťapuchová
Quality Control Manager
Mgr. Eliška Buštíková
Laboratory Technician
Ing. Petra Česnek, Ph.D.
Administrative Support
CTEF represents a unit manufacturing advanced therapy medicinal products (ATMPs) including cell therapy and tissue engineered products. Products are manufactured from viable autologous or allogeneic cells and they can also contain non cellular components (chemical/biological compounds, matrices, scaffold etc.). All manufacturing and quality control activities at CTEF are carried out in accordance with the principles of cGMP to provide the authorization for the manufacture and investigation of all medical products within the clinical trials. Environmental Monitoring and Assessment is conducted continuously during the production processes.
The facility provides licensed manufacturing and testing of cGMP grade medicinal products for pre-clinical and clinical trials and is available to academic and private sector scientists, taking care of the project license and authorization process. In cooperation with Masaryk University, CTEF also provides support in the translation of research and development outcomes into a manufacturing setting.
CTEF has ISO 9001 certification (quality management system) and GMP manufacture permit from SÚKL.
Specific products: Virus-specific lymphocytes (VSL), peripheral blood mononuclear cells (PBMC), chimeric antigen receptor T-cells (CAR-T cells), human embryonic stem cells (hESC), human induced pluripotent stem cells (hiPSC)
The facility cooperates with many partners, including: Masaryk University, Brno, University Hospital Brno; Olomouc University Hospital; Institute of Hematology and Blood Transfusion, Prague; The Institute of Genetic Medicine, Newcastle, UK; Mayo – Center for Regenerative Medicine, Rochester, USA; Leibniz Research Laboratories for Biotechnology and Artificial Organs, Hannover, Germany