Module Name Drug Dosage Forms Design 2
Module level, if applicable 2nd Year
Code, if applicable SFA-435
Semester (s) in which the module is taught 4th semester
Person responsible for the module Prof. Dr. apt. Yandi Syukri, M.Si
Lecturer(s) Prof. Dr. apt. Yandi Syukri, M.Si

Dr. apt. Lutfi Chabib, MSc.

Dr. apt. Siti Zahliyatul Munawiroh
Language Bahasa Indonesia and English
Relation to curriculum Compulsory
Types of teaching and learning Class size Attendance time (hours per week per semester) Forms of active participation Workload  
Teaching, discussion and project development

 

 50 – 60 

 

 2

 

 Discussion Lecture: 2 (hours) x 14 (meeting) 28
  Preparation and project assignment 4 (hour) x 14 (meeting) 64
Total workload 84 hours
ECTS 3 ECTS
Credit points 2 CU
Requirements according to examination regulations Minimum attendance at lectures is 75% (according to UII regulation).
Recommended prerequisites Drug Dosage Forms Design 1
Related course  
Module objectives/intended learning On successful completion of the course students should be able to:

  1. 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.
  2. Develop and solve problems of pharmaceutical preparation formulas covering aspects of biopharmaceutical and bioequivalence.
  3. Explain concepts and perform preformulation (selection, design, materials and quality control of packaging for liquid, semi-solid and gas preparations).
  4. Design liquid, semi-solid and gas dosage formulas.
  5. 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.
Study and examination requirements and forms of examination Midterm and final term, project assignment and presentation
Media employed Blended Learning
Reading lists
  1. Ansel, HC., Allen, LV., Popovich, NG., 2006, Pharmaceutical Dosage Form and Drug Delivery System, 8th edition, Lippincott William & Wilkin, USA.
  2. Swarbrick, J (Ed)., 2007, Encyclopedia of Pharmaceutical Technology, Informa Healthcare, USA