Farmasötik Toksikoloji Tezli Yüksek Lisans Diploması

Have knowledge about the adverse effects of chemical, biological and physical factors on living organisms and the environment, the conditions of occurrence of these effects and prevention and prevention of these effects. Fate of toxic agents in organism and environment, prediction and risk assessment of possible toxic effects, determination of short and long term toxic effects in target systems, toxic effect mechanisms, toxicity measurement methods, toxicity diagnosis and treatment. Has knowledge about the nutrients, natural components and the allowable levels of additives and the adverse effects of environmental pollutants and toxic substances in foods. Has knowledge about the important and specific issues of toxicology such as safe use of drugs and chemicals, risk assessment of toxic factors exposed in the workplace environment, disaster toxicology. To be able to determine the toxicity-causing factors including the drugs and the toxic effects in the organism by using different information technologies, field-specific devices and research methods. Have knowledge about safe drug use in risky groups. Interprets current information in the field of toxicology by integrating it with information from different disciplines. Gains the ability to conduct independent research by using information from different sub-branches of toxicology. It conducts its activities in accordance with all ethical principles and rules and supports the development of ethical values.

Course success grade is given to students for each course at the end of the semester they are registered. Course success grade is obtained by evaluating the success of the student during the semester (midterm exams, homework, applied studies, projects, laboratory and similar studies) and the general exam. Program courses must be successfully completed in two years at most, with a minimum GPA of 2.50. In order to graduate from the Pharmaceutical Toxicology Masters Program with Thesis, the student must complete at least 21 credits and 120 ECTS (At least seven courses, seminar course and thesis study). The seminar course and thesis work are non-credit and evaluated as successful / unsuccessful. Even if the student has credit transfer courses, he / she has to take at least half of the total credits required by his / her program from his / her own program. If the advisor deems appropriate and necessary, courses from other programs can also be selected. The Lokman Hekim University Graduate Education and Examination Regulations are taken as basis in the evaluation of the students course success.

Student applications, admissions and final registrations to the Pharmaceutical Toxicology Masters Program with Thesis are made in accordance with the Lokman Hekim University Health Sciences Institute Graduate Education Instruction. In addition, the special conditions required for the students who apply with the recommendation of the Department and the decision of the Institute Administrative Board before each application period, the entrance exam place and date are determined and announced before the application. Graduates of the Faculty of Pharmacy, Faculty of Medicine, Faculty of Science, Biology and Chemistry Departments and those approved by the Academic Board of the Department of Undergraduate / Masters Degree can apply to the Pharmaceutical Toxicology Masters Program. Turkish or foreign students who have completed their undergraduate program in foreign countries must have an equivalence or recognition certificate from the Higher Education Council. For the applications to be made to the program, it is required to have the ALES (SAY / EA) score determined by the Institute Board, provided that it is not less than 55. Students who meet the application requirements are taken to the scientific evaluation exam (written and / or interview). The calculation of the general success grade is made by considering the ALES score, the undergraduate graduation grade average and the results of the Scientific evaluation exam. The student is entitled to final registration within the quota specified according to the general success grade ranking.

Pharmaceutical industry especially Pharmacovigilance, Regulatory Affairs and R&D units The Ministry of Health Medicines and Medical Devices different units located mainly within Turkey Pharmacovigilance Center Authority Drug and Poison Information Centers Forensic toxicology laboratories Reference laboratories and risk assessment units of the Ministry of Environment and Urbanization and the Ministry of Food, Agriculture and Livestock Pharmaceutical Toxicology Departments in Pharmacy Faculties

Qualification is continuous