Module Name Pharmaceutical Dosage Form Analysis
Module level, if applicable 2nd year
Code, if applicable SFA-438
Semester (s) in which the module is taught Fourth semester
Person responsible for the module apt. Ardi Nugroho, 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
Teaching 50 3 Collaborative discussion Lecture: 3 (hour) x 14 (meeting) 52
Discussion Presentation Preparation and follow up 5 (hour) x 14 (self-learning) 70
Total workload 122
4.36 ECTS
Credit points 3 CU
Requirements according to examination regulations Minimum attendance at lectures is 75% (according to UII regulation). Final score is evaluated based on assignment and reports (40%); discipline (10%), and exam (50%)  
Recommended prerequisites Pharmaceutical Analysis
Related course –
Module objectives/intended learning By the end of this course students should be able to:

  1. Apply professional attitude and ethical manners during the lecture.. 
  2. Examine chromatographic methods for analyzing analyte.
  3. Study spectroscopic methods for analyzing analyte.
  4. Design validation of bioanalysis methods.
  5. Design machine learning in pharmaceutical field and particle characterization.
Content The course will cover: 

The analytical methods are fluorometer spectrophotometry, atomic absorption spectroscopy, infrared spectroscopy, advanced instruments in the pharmaceutical field, gas and liquid chromatography, bioanalytical validation, particle characterization.
Study and examination requirements and forms of examination Mid-term, Final term, presentation, quiz, assignment, and collaborative discussion
Media employed Text books, slides (power points), and video
Reading lists
  1. Christian, GD, 2004, Analytical Chemistry, Sixth Edition, John Wiley and Sons Inc, New York.
  2. Harris, D.C., 2010, Quantitative Chemical Analysis, Eighth Ed., W.H. Freeman and Company, New York
  3. Pavia, DL., Lampman, GM., Kriz, GS., 2001, Introduction to Spectroscopy A guide for students of organic chemistry, third edition, Thomson Learning, Inc., USA.
  4. Snyder, LR., Kirkland, JJ., Dolan, JW., 2010, Introduction to Modern Liquid Chromatography, third edition, John Wiley & Sons, Inc., USA.
  5. Kompendia (FI, USP, BP) dan standar lain (ICH, AOAC).
  6. Food and Drug Administration, 2018, Guidance for Industry: Bioanalytical Method Validation, Department of Health and Human Services.
  7. Miller, J.N. and Miller, J.C., 2005, Statistics and Chemometrics for Analytical Chemistry, Pearson Education Limited, Essex England. 
  8. Fifield, FW., Kealey D., 2000, Principles and Practice of Analytical Chemistry, fifth edition, Blackwell Scince Ltd., UK. 
  9. Setiabudi A., Hardian R., Mudzakir A., 2012, Karakterisasi Material, UPI Press, Jakarta