Module Name Practical on Pharmaceutical Dosage Form Analysis
Module level, if applicable 2nd  year
Code, if applicable SFA-442
Semester (s) in which the module is taught Fourth semester
Person responsible for the module apt. Ari Wibowo, M.Sc.
Lecturer(s) apt. Ari Wibowo, M.Sc.

apt. Ardi Nugroho, M.Sc.
Language English- Indonesia
Relation to curriculum Compulsory course
Types of teaching and learning Class size Attendance time (hours per week per semester) Forms of active participation Workload
Practical course 30 3 Collaborative discussion Laboratory Practice 3 (hours) x 14 (meeting) 42
Collaborative Learning  Collaborative Problem Solving
Total workload 42
ECTS 1.5 ECTS
Credit points 1 CU
Requirements according to examination regulations Minimum attendance at lectures is 75% (according to UII regulation). Final score is evaluated based on laboratory practices and reports (55%), discipline (15%), and exam (30%)  
Recommended prerequisites –
Related course –
Module objectives/intended learning By the end of this course students should be able to:

  1. Apply responsibility and discipline in carrying out the practice.
  2. Carry out occupational safety and health techniques in the laboratory.
  3. Analyze compounds using spectroscopy and chromatography methods.
  4. Analyze and evaluate data based on applicable guidelines
Content The course will cover: 

Safety and health in the laboratory, analytical methods of atomic absorption spectroscopy, infrared spectroscopy, gas and liquid chromatography, analytical derivative techniques, validation of bioanalytical methods.
Study and examination requirements and forms of examination Worksheet assessment, quiz, assignment, and final exam
Media employed Text books, slides (power points), and video
Reading lists
  1. Harris, D.C., 2010, Quantitative Chemical Analysis, Eighth Ed., W.H. Freeman and Company, New York
  2. Pavia, DL., Lampman, GM., Kriz, GS., 2001, Introduction to Spectroscopy A guide for students of organic chemistry, third edition, Thomson Learning, Inc., USA.
  3. Snyder, LR., Kirkland, JJ., Dolan, JW., 2010, Introduction to Modern Liquid Chromatography, third edition, John Wiley & Sons, Inc., USA.
  4. Kompendia (FI, USP, BP) dan standar lain (ICH, AOAC).
  5. Food and Drug Administration, 2018, Guidance for Industry: Bioanalytical Method Validation, Department of Health and Human Services.
  6. Miller, J.N. and Miller, J.C., 2005, Statistics and Chemometrics for Analytical Chemistry, Pearson Education Limited, Essex England