GAZI UNIVERSITY INFORMATION PACKAGE - 2019 ACADEMIC YEAR

COURSE DESCRIPTION
PARENTERAL SOLUTION AND OTHER STERIL PRODUCT TECHNOLOGY/FTE-1050
Course Title: PARENTERAL SOLUTION AND OTHER STERIL PRODUCT TECHNOLOGY
Credits 3 ECTS 7
Semester 1 Compulsory/Elective Elective
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://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
Learning of the basic principles in parenteral solutions
Learning of the the methods of preparing enjaktabl water
Understanding of the formulation of small and large volume of parenterals






 -- MODE OF DELIVERY
  The mode of delivery of this course is 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  Basic principles in parenteral solutions,
2. Week  The methods of preparing enjaktabl water
3. Week  The methods of preparing enjaktabl water
4. Week  Preparing of enjectabl water by distillation and reverse osmoz method
5. Week  Formulation of small and large volume of parenterals, quality control of parenteral products
6. Week  Formulation of small and large volume of parenterals, quality control of parenteral products
7. Week  Production in aseptic conditions
8. Week  Production of steril powders
9. Week  Production of steril powders
10. Week  The main points in the preparation of parenteral products
11. Week  Quality controls during the production of parenteral products
12. Week  In vivo and in vitro proygen tests
13. Week  Quality control in parenteral products
14. Week  Quality control in parenteral products
15. Week  
16. Week  
 -- RECOMMENDED OR REQUIRED READING
  Remington: The Science and Practice of Pharmacy, Ed: AR Gennaro, 20th Ed., Lippincott Williams & Wilkins, 2002.
 -- 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
1
10
 Exercises
0
0
 Projects
1
50
 Practice
0
0
 Quiz
0
0
 Contribution of In-term Studies to Overall Grade  
60
 Contribution of Final Examination to Overall Grade  
40
 -- WORKLOAD
 Efficiency  Total Week Count  Weekly Duration (in hour)  Total Workload in Semester
 Theoretical Study Hours of Course Per Week
14
2
28
 Practising Hours of Course Per Week
0
0
0
 Reading
5
4
20
 Searching in Internet and Library
4
4
16
 Designing and Applying Materials
0
0
0
 Preparing Reports
0
0
0
 Preparing Presentation
4
10
40
 Presentation
5
10
50
 Mid-Term and Studying for Mid-Term
1
10
10
 Final and Studying for Final
1
11
11
 Other
0
 TOTAL WORKLOAD: 
175
 TOTAL WORKLOAD / 25: 
7
 ECTS: 
7
 -- 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