Module Name Practical on Aseptic Formulation and Technology
Module level, if applicable 3rd year
Code, if applicable SFA-659
Semester (s) in which the module is taught Sixth semester
Person responsible for the module Dr. apt. Lutfi Chabib, M.Sc.
Lecturer(s) Dr. apt. Lutfi Chabib, 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 (45%), discipline (15%), and exam (40%)  
Recommended prerequisites Aseptic Formulation and Technology
Related course –
Module objectives/intended learning By the end of this course students should be able to:

  1. apply an attitude of responsibility, dedication, togetherness and discipline based on sincerity, honesty and integrity in the manufacture of solid preparations carefully and thoroughly.
  2. work together in groups
  3. preformulation, design and packaging of sterile preparations
  4. make sterile preparations
  5. carry out quality control of sterile preparations
Content The course will cover: 

  1. Preformulation of sterile preparations
  2. Sterile dosage formulation
  3. Manufacturing of sterile preparations
  4. Quality control of sterile preparations
  5. Technology and formulation of small and large volume injection preparations
  6. Technology and formulation of eye drops and eye ointments
  7. Technology and formulation of nasal drops and ear drops
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. Niazi, S. K. (2009). Handbook of pharmaceutical manufacturing formulations. CRC press.
  2. Akers, M. J. (2016). Sterile drug products: formulation, packaging, manufacturing and quality (Vol. 208). CRC Press.


Module Name

 Practical on Aseptic Formulation and Technology
Module level, if applicable 3rd year
Code, if applicable SFA-659
Semester (s) in which the module is taught Sixth semester
Person responsible for the module Dr. apt. Lutfi Chabib, M.Sc.
Lecturer(s) Dr. apt. Lutfi Chabib, 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
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 (45%), discipline (15%), and exam (40%)  
Recommended prerequisites Aseptic Formulation and Technology
Related course –
Module objectives/intended learning By the end of this course students should be able to:

  1. apply an attitude of responsibility, dedication, togetherness and discipline based on sincerity, honesty and integrity in the manufacture of solid preparations carefully and thoroughly.
  2. work together in groups
  3. preformulation, design and packaging of sterile preparations
  4. make sterile preparations
  5. carry out quality control of sterile preparations
Content The course will cover: 

  1. Preformulation of sterile preparations
  2. Sterile dosage formulation
  3. Manufacturing of sterile preparations
  4. Quality control of sterile preparations
  5. Technology and formulation of small and large volume injection preparations
  6. Technology and formulation of eye drops and eye ointments
  7. Technology and formulation of nasal drops and ear drops
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. Niazi, S. K. (2009). Handbook of pharmaceutical manufacturing formulations. CRC press.
  2. Akers, M. J. (2016). Sterile drug products: formulation, packaging, manufacturing and quality (Vol. 208). CRC Press.