GAZI UNIVERSITY INFORMATION PACKAGE - 2019 ACADEMIC YEAR

COURSE DESCRIPTION
SEMINAR/FTE-1002
Course Title: SEMINAR
Credits 0 ECTS 2
Semester 1 Compulsory/Elective Compulsory
COURSE INFO
 -- LANGUAGE OF INSTRUCTION
  Turkish
 -- NAME OF LECTURER(S)
  Prof.Dr.F.Acartürk, Prof.Dr.F.Tırnaksız, Prof.Dr.S.Takka, Assoc.Prof.Dr.Z.Ş.Teksin, Assoc.Prof.Dr.T.İnceçayır, Assoc.Prof.Dr.S.İ.Tamer, Assoc.Prof.Dr.F.T.Demiröz
 -- WEB SITE(S) OF LECTURER(S)
  http://www.websitem.gazi.edu.tr/site/tfigen
 -- EMAIL(S) OF LECTURER(S)
  acarturk@gazi.edu.tr, tfigen@gazi.edu.tr, takka@gazi.edu.tr, zsteksin@gazi.edu.tr, tincecayir@gazi.edu.tr, ilbasmis@gazi.edu.tr, fatmanur@gazi.edu.tr
 -- LEARNING OUTCOMES OF THE COURSE UNIT
Be able to establish literature search
Be able to read, understand and make comment about the literature
Be able to prepare and present of the research subject
 -- MODE OF DELIVERY
  Face to face
 -- PREREQUISITES AND CO-REQUISITES
   There is no prerequisite or co-requisite for this course
 -- RECOMMENDED OPTIONAL PROGRAMME COMPONENTS
  There is no recommended optional programme component for this course.
 --COURSE CONTENT
1. Week  Determining seminer subject
2. Week  Literature survey
3. Week  Literature survey
4. Week  Literature survey
5. Week  Literature survey
6. Week  Collecting data
7. Week  Collecting data
8. Week  Collecting data
9. Week  Collecting data
10. Week  Collecting data
11. Week  Collecting data
12. Week  Preparation of the presentation
13. Week  Preparation of the presentation
14. Week  Presentation
15. Week  
16. Week  
 -- RECOMMENDED OR REQUIRED READING
  Releated articles and references
 -- PLANNED LEARNING ACTIVITIES AND TEACHING METHODS
  Seminary, recitation
 -- WORK PLACEMENT(S)
  -
 -- ASSESSMENT METHODS AND CRITERIA
 
Quantity
Percentage
 Mid-terms
0
0
 Assignment
0
0
 Exercises
0
0
 Projects
0
0
 Practice
0
0
 Quiz
0
0
 Contribution of In-term Studies to Overall Grade  
0
 Contribution of Final Examination to Overall Grade  
100
 -- WORKLOAD
 Efficiency  Total Week Count  Weekly Duration (in hour)  Total Workload in Semester
 Theoretical Study Hours of Course Per Week
0
 Practising Hours of Course Per Week
0
 Reading
6
4
24
 Searching in Internet and Library
6
4
24
 Designing and Applying Materials
0
 Preparing Reports
0
 Preparing Presentation
1
1
1
 Presentation
1
1
1
 Mid-Term and Studying for Mid-Term
0
 Final and Studying for Final
0
 Other
0
 TOTAL WORKLOAD: 
50
 TOTAL WORKLOAD / 25: 
2
 ECTS: 
2
 -- 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