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Registration And R&D

Regulatory Affairs and Product Development departments of Company finalized received R&D projects and obtained support from the Scientific and Technological Research Agency Council of Turkey and KOSGEB. New projects are continuously planned for new products.

As a research and development oriented generic pharmaceutical company, R&D department has a unique role in attaining both short and long-term goals of Tum Ekip. Regulatory Affairs and Product development departments, together develop the new registration files. Tum Ekip laboratories and all the production facilities supports these projects accordingly.

The main purpose of R&D department is to develop essentially similar pharmaceutical dosage forms needed in clinics and to present high quality, safe and affordable generic solutions, attaching paramount importance to quality and ensuring such quality during the design process. To this end, the R&D department develops injectable dosage forms in compliance with the guidelines of International Conference on Harmonization (ICH). The R&D laboratories, including the pilot manufacturing lab, are equipped with state-of the-art technology and the experiments are conducted in accordance with Good Manufacturing Practices (cGMP) and Good Laboratory Practices (cGLP).