GAZI UNIVERSITY INFORMATION PACKAGE - 2019 ACADEMIC YEAR

COURSE DESCRIPTION
MASTER SCIENCE THESIS PERIOD/1110999
Course Title: MASTER SCIENCE THESIS PERIOD
Credits 0 ECTS 30
Semester 3 Compulsory/Elective Compulsory
COURSE INFO
 -- LANGUAGE OF INSTRUCTION
  Turkish
 -- NAME OF LECTURER(S)
  Supervisor
 -- WEB SITE(S) OF LECTURER(S)
  http://www.websitem.gazi.edu.tr/site/acarturk
 -- EMAIL(S) OF LECTURER(S)
  acarturk@gazi.edu.tr
 -- LEARNING OUTCOMES OF THE COURSE UNIT
Be able to review literature about thesis subject
Be able to collect, analyse, make comments and use the data
Be able to plan the research period
Be able to discuss the problems and solutions of the research
 -- MODE OF DELIVERY
  The mode of delivery of this course is face to face
 -- PREREQUISITES AND CO-REQUISITES
  To be pharmacy scholl graduates
 -- RECOMMENDED OPTIONAL PROGRAMME COMPONENTS
  There is no recommended optional programme component for this course.
 --COURSE CONTENT
1. Week  Determination of the thesis subject
2. Week  Literature survey on the suggested subject
3. Week  Literature survey on the suggested subject
4. Week  Literature survey on the suggested subject
5. Week  Planning of a research
6. Week  Planning of a research
7. Week  Carrying out studies for the research and planning of the research
8. Week  Carrying out studies for the research and planning of the research
9. Week  Implementation of plans and providing the necessary materials and supplies
10. Week  Implementation of plans and providing the necessary materials and supplies
11. Week  Carrying out research plan and performing the experiments
12. Week  Carrying out research plan and performing the experiments
13. Week  Evaluation and discussion of the reported data
14. Week  Reporting data
15. Week  
16. Week  
 -- RECOMMENDED OR REQUIRED READING
  Related articles and books
 -- PLANNED LEARNING ACTIVITIES AND TEACHING METHODS
  Lecture, Question & Answer, Demonstration, Drill - Practise
 -- WORK PLACEMENT(S)
  -
 -- ASSESSMENT METHODS AND CRITERIA
 
Quantity
Percentage
 Mid-terms
0
0
 Assignment
0
0
 Exercises
0
0
 Projects
0
0
 Practice
1
40
 Quiz
0
0
 Contribution of In-term Studies to Overall Grade  
40
 Contribution of Final Examination to Overall Grade  
60
 -- WORKLOAD
 Efficiency  Total Week Count  Weekly Duration (in hour)  Total Workload in Semester
 Theoretical Study Hours of Course Per Week
14
25
350
 Practising Hours of Course Per Week
11
20
220
 Reading
10
8
80
 Searching in Internet and Library
14
6
84
 Designing and Applying Materials
2
3
6
 Preparing Reports
4
3
12
 Preparing Presentation
0
 Presentation
0
 Mid-Term and Studying for Mid-Term
0
 Final and Studying for Final
0
 Other
0
 TOTAL WORKLOAD: 
752
 TOTAL WORKLOAD / 25: 
30.08
 ECTS: 
30
 -- COURSE'S CONTRIBUTION TO PROGRAM
NO
 PROGRAM LEARNING OUTCOMES
1
2
3
4
5
1Posesses extensive knowledge accumulation on the field of Pharmaceutical Technology, learns pre-formulations of all pharmaceutical dosage forms, formulation designs and in vitro/in vivo evaluations of formulations.X
2Gains the capability of following up novalities in technology, and posesses the capability of literature search, evaluation and interpretation on the fields of Pharmacy.X
3Gains the capability of patent search and evaluation and patenting regarding the formulations of active drug ingredient, dosage forms and preparation technologies.X
4Learns sufficient knowledge on the the field of laboratory, pilot batch and industrial scale productions, quality controls, quality assurance system, good manufacture practice (GMP) and stability assurance of all dosage forms.X
5Learns the knowledge satisfying the capability level for designing original and generic drugs, evaluating process validation and quality assurance.X
6Learns the interpretation, statistical evaluation and practical application of the research results.X
7Posesses the knowledge on new drug delivery systems and posesses the knowledge and capacity on targetting these systems at a level of an expert.X
8Learns designing, formulations, preparation techniques, physical and chemical stabilities of biotechnological products.X
9Gains the capability of finding solutions to the problems encountered during research. He/she gains the capability of analytical thinking. He/she gains the capability of publishing the experimental results in the national/international journals.X
10Gains the capability of following and interpretion of important wold health organizations (FDA, EMA, ICH and WHO) and official reference books (pharmacopoeia etc.). As a result, he/she transfers his/her knowledge to the field of Pharmaceutical Technology, and develops new approaches.X