R&D Center

Pharmaceutical research and development studies; It always aims to provide the service of human health by developing effective, safe, patient adaptation and innovative economic products that will enable patients to live a healthier and quality life all over the world and continues its activities within this scope. Our R&D department; analytical development laboratory (Instrumental analysis laboratories, wet chemistry laboratories), preformulation and formulation laboratory, pilot production and stability areas. In the project teams working in our R&D department; researchers are involved in scientific competence.

Our products in solid, semi-solid and liquid dosage forms are developed in our own R&D laboratory. Patent screening and evaluation studies, effective substance evaluation, analysis and approval studies, formulation and analytical method development, laboratory and pilot productions, process and analytical method validations, product improvement studies, new product stability studies, preparation of license files in CTD format are carried out in accordance with the International Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP) rules determined by the World Health Organization (WHO) within the framework of national and international regulations and guidelines. Patent applications are made in order to protect our intellectual and industrial rights. Some of these projects are carried out within the scope of TUBITAK-TEYDEB Industrial Research and Development Projects Support Program.

Our Specialties

Detailing formulation and process engineering
API sourcing across our select network of suppliers
Supplier qualification services analytical characterization of raw materials, intermediates and drugs
Expanding the production process

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