Drug Analysis and Control Lab.


Drug development requires preclinical studies prior to IND application which should be performed in GLP certified laboratories. There is no GLP certified preclinical testing facility in Turkey, which constitutes a significant barrier for new molecular entity development. IBG has established Drug Analysis and Control Laboratories which are in compliance with GLP regulations and Quality Management System.

Good Laboratory Practice (GLP) in an internationally recognized indicator of technical competence in pre-clinical studies. By providing official recognition of the competence of laboratories, it ensures a convenient method for identifying and selecting reliable test and analysis services for institutions in need of preclinical work for their molecules.

Click here for contact procedure with sponsors.

Click here for the procedure including test material accepting criteria.

Group Members

Drug Analysis and Control Lab.

ALEV TAŞÇIOĞLU ALİYEV Researcher  alev.aliyev@ibg.edu.tr

Ayşegül DEMİRTAŞ Quality Assurance Department Manager  aysegul.demirtas@ibg.edu.tr
+90 232 299 41 00 (2401)
0 232 299 41 44

Ezgi ERBAY Quality Assurance Technician  ezgi.erbay@ibg.edu.tr

Berrak SOHTORİK Support Archieve and Documentation  berrak.sohtorik@ibg.edu.tr
+90 232 299 41 00 (3801)

Selin YEŞİL Microbiology Laboratory Unit Responsible  selin.yesil@ibg.edu.tr

Melda Zeynep GÜRAY Biopharmaceuticals Laboratory Unit Responsible  melda.guray@ibg.edu.tr
+90 232 299 41 00 (2901)

Güzide İdil TİLMENSAĞIR Biopharmaceuticals Laboratory Research Technician  idil.tilmensagir@ibg.edu.tr

Former Members

Tuba KARAMAN ODUNCU Research Technician  tuba.karaman@ibg.edu.tr


Drug Analysis and Control Lab.