P.Ç. 1 Has the knowledge of accessing scientific information in the field of pharmacy, monitoring and evaluating the current literature.
P.Ç. 2 Has an advanced level of knowledge about drug raw materials and drug forms.
P.Ç. 3 Cooperates with people from related disciplines during the stages of collecting, interpreting, applying and announcing the data related to the field of pharmacy.
P.Ç. 4 Uses the information and equipment related to the administration and administration of the drug, provides the supervision and supervision duty and rational and safe drug use and provides the pharmaceutical care service.
P.Ç. 5 Gains the administrative and technical skills in every field where the profession of Pharmacy is given responsibility by law and makes pharmacy design according to the rules.
P.Ç. 6 Uses computer programs and advanced technologies related to the field of pharmacy.
P.Ç. 7 Produces solutions in the field of pharmacy profession according to scientific data / evidence.
P.Ç. 8 Makes the recognition, quality, control and standardization of the drug.
P.Ç. 9 Plans, manages and monitors the process for the development of the employees working under their responsibility within the framework of a project.
P.Ç. 10 Carries out a study independently by using his advanced knowledge in the field of pharmacy and takes responsibility as a team member in cooperation with other professional groups working in this field.
P.Ç. 11 Demonstrates that he / she has adopted lifelong learning, is open to development and maintains this behavior.
P.Ç. 12 Evaluates the knowledge and skills acquired in the field of pharmacy with a critical approach.
P.Ç. 13 Follows and evaluates the national and international developments in the field of pharmacy.
P.Ç. 14 Documents and records professional activities and practices safely.
P.Ç. 15 Transfers information to the patient, the health personnel and the society in all matters related to the drug.
P.Ç. 16 Uses English as a foreign language to monitor and communicate pharmaceutical innovations.
P.Ç. 17 Informs the concerned people and institutions about the quality assurance of pharmaceutical products.
P.Ç. 18 Takes part in every step of the preparation of pharmaceutical products, from the preparation of pharmaceutical raw materials to the design and manufacture of pharmaceutical forms.
P.Ç. 19 Comprehends and regulates drug licensing conditions, data protection and patent issues.
P.Ç. 20 Acts in accordance with the legislation and professional ethics rules related to his / her duties, rights and responsibilities as individuals.
P.Ç. 21 Has sufficient awareness about the individual and public health, environmental protection and occupational safety.