Mihriban Incmen

 Responsible for the drug registration procedures.  Application process to the Ministry of Health for registration.  Preparation registration files in CTD format.  Preparation of registration, renewal, and variation dossiers and follow up at level of the Ministry of Health.  To prepare the validation protocoles and reports.

 Arranging the shifts programs.  Collecting and controlling the data of analysis for products/semi products.  Working and calibrating the working standards and reference standards.  Collecting and controlling the data of analysis for raw materials.  Validation and operating the new methods for raw materials and finished products

have responsibility for finding new suppliers for raw materials from China, Far East or European Countries, make contacts with them, test the quality of their products while having samples and finally giving orders to the corresponding companies and passing the documents to Import Department have responsibility for making contacts with current suppliers from China, Far East or European Countries, checking the quantities of the goods from the stocks and giving the orders to corresponding companies.