GAZI UNIVERSITY INFORMATION PACKAGE - 2019 ACADEMIC YEAR
Program Learning Outcomes
| PROGRAM LEARNING OUTCOME |
| KNOWLEDGE |
| Theoretical, Factual |
| - Follow the development as having the knowledge and skills in the field of industrial pharmacy, transfer the information to the pharmaceutical industry and develop new approaches in this area. |
| - Gains the ability to acess and apply to the health orginazations guidlines such as FDA, EMA, WHO. |
| - Learns the concept of systematic R&D, techniques, tools and scale up in drug development. |
| - Learns the concept and application of drug formulation development by using quality by design (QbD) and process analytical technology (PAT). |
| - Learns the concept of original and generic drug and the evaluation and interpretation of the study design of bioavalability/bioequivalance |
| - Posess the knowledge and skill about the analytical techniques, method development and validation in the industrial pharmacy. |
| SKILLS |
| Cognitive, Practical |
| COMPETENCIES |
| Ability to work independently and take responsibility |
| - Follow the development as having the knowledge and skills in the field of industrial pharmacy, transfer the information to the pharmaceutical industry and develop new approaches in this area. |
| Learning Competence |
| - Follow the development as having the knowledge and skills in the field of industrial pharmacy, transfer the information to the pharmaceutical industry and develop new approaches in this area. |
| - Gains the ability to acess and apply to the health orginazations guidlines such as FDA, EMA, WHO. |
| - Preparation and evaluation of the CTD format of the license application to the Turkish Drug and Medical Devices Agency and learn the types of license application made to the other health organizations |
| - Posess the knowledge on the total quality management, GMP, GLP, GSP, QA / QC, process validation, analytical validation and qualification in in the pharmaceutical industry. |
| - Learns the concept of systematic R&D, techniques, tools and scale up in drug development. |
| - Posseses the ability to evaluate and interprete the drug patent databases (TPE, EPO, WIPO etc.) |
| - Posess the knowledge and skill about the analytical techniques, method development and validation in the industrial pharmacy. |
| - Get the application skill in the releated area by pursuing knowledge in the field of pharmacovigilance and pharmacoeconomics. |
| - Develops new approaches to potential problems and bring solutions by using the knowledge in the releated area. |
| Communication and Social Competence |
| Field-based Competence |
| - Gains the ability to acess and apply to the health orginazations guidlines such as FDA, EMA, WHO. |
| - Preparation and evaluation of the CTD format of the license application to the Turkish Drug and Medical Devices Agency and learn the types of license application made to the other health organizations |
| - Posess the knowledge on the total quality management, GMP, GLP, GSP, QA / QC, process validation, analytical validation and qualification in in the pharmaceutical industry. |
| - Learns the concept and application of drug formulation development by using quality by design (QbD) and process analytical technology (PAT). |
| - Posseses the ability to evaluate and interprete the drug patent databases (TPE, EPO, WIPO etc.) |
| - Learns the concept of original and generic drug and the evaluation and interpretation of the study design of bioavalability/bioequivalance |
| - Get the application skill in the releated area by pursuing knowledge in the field of pharmacovigilance and pharmacoeconomics. |
| - Develops new approaches to potential problems and bring solutions by using the knowledge in the releated area. |