COURSE INFORMATION
Module Name | Drug Dosage Forms Design 2 | |||
Module Level, if applicable | 2nd year | Types of teaching and learning | Teaching, Discussion and Project Development | |
Code, if applicable | SFA-435 | Class size | 50 – 60 | |
Semester | 4th Semester | Attendance time (hours per week per semester) | 2 h | |
Person responsible for the module | Prof. Dr. apt. Yandi Syukri, M.Si | Forms of active participation | Discussion | |
Lecturer(s) | Prof. Dr. apt. Yandi Syukri, M.Si
Dr. apt. Lutfi Chabib, MSc. Dr. apt. Siti Zahliyatul Munawiroh |
Workload | Lecture: 2 (hour) x 14 (meeting) = 28
Preparation and follow up 4 (hour) x 14 (self-learning) = 56 |
|
Language | English- Indonesia | Total workload | 84 hours | |
Relation to curriculum | Compulsory course | Credit points | 2 CU |
REQUIREMENTS
Requirements according to examination regulations | Minimum attendance at lectures is 75% (according to UII regulation). |
Recommended prerequisites | Drug Dosage Forms Design 1 |
Related course | – |
Study and examination requirements and forms of examination | Midterm and final term, project assignment and presentation |
MODULE OBJECTIVES/INTENDED LEARNING
By the end of this course students should be able to:
- Apply an attitude of responsibility, dedication, togetherness and discipline based on honesty, honesty and integrity in the careful and thorough manufacture of liquid, semi-solid and gas preparations and the development of pharmaceutical preparations.
- Develop and solve problems of pharmaceutical preparation formulas covering aspects of biopharmaceutical and bioequivalence.
- Explain concepts and perform preformulation (selection, design, materials and quality control of packaging for liquid, semi-solid and gas preparations).
- Design liquid, semi-solid and gas dosage formulas.
- Explain and control the quality of pharmaceutical preparations (liquid, semisolid and gaseous) including the stability test of preparations
CONTENT
This course aims to support Program Learning Outcomes in the form of professional and ethical abilities, research and development as well as skills in making pharmaceutical preparations. In this course, students learn about various aspects: pre-formulation, formulation, manufacture, quality control and packaging of liquid, semi-solid and gas preparations; pharmaceutical product stability; biopharmaceutical studies; and drug product bioequivalence test.
MEDIA EMPLOYED
Blended Learning
READING LISTS
- Ansel, HC., Allen, LV., Popovich, NG., 2006, Pharmaceutical Dosage Form and Drug Delivery System, 8th edition, Lippincott William & Wilkin, USA.
- Swarbrick, J (Ed)., 2007, Encyclopedia of Pharmaceutical Technology, Informa Healthcare, USA