Module Name Pharmaceutical Industry
Module level, if applicable 4th Year
Code, if applicable SFA-655
Semester (s) in which the module is taught 7th semester
Person responsible for the module Dr. apt. Siti Zahliyatul Munawiroh
Lecturer(s) Dr. apt. Siti Zahliyatul Munawiroh

Prof. Dr. apt. Yandi Syukri, MSc.

apt. Bambang H. Nugroho, MSc.

apt. Oktavia Indrati, MSc.
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 2
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 sincerity, honesty and integrity in making pharmaceutical preparations carefully and thoroughly.
  2. Comprehend the theory of Good Manufacturing Practice (GMP) including traditional medicine and cosmetics.
  3. Comprehend the design, construction, support facilities and functions of existing equipment in the pharmaceutical industry and their qualifications.
  4. Comprehend validation and qualifications in the pharmaceutical industry.
  5. Able to know the aspects of pharmaceutical halal products
Content This course is a compulsory subject that is taken with the prerequisite for drug Dosage Forms Design 2. This course aims to support the Program learning outcomes in the form of skills in knowledge of the scope of pharmaceutical work, legal knowledge and pharmaceutical ethics in the pharmaceutical industry. This course also discusses principles of work safety as well as professional and ethical leadership and management in the pharmaceutical industry.
Study and examination requirements and forms of examination Midterm and final term, project assignment and presentation
Media employed Blended Learning
Reading lists
  1. Anonim, 2012, Peraturan Kepala Badan Pengawas Obat dan Makanan Republik Indonesia Nomor HK.03.1.33.12.12.8195 Tahun 2012 Tentang Penerapan Pedoman Cara Pembuatan Obat yang Baik, Jakarta.
  2. Anonim, 2013, Petunjuk Operasional Penerapan Pedoman Cara Pembuatan Obat Yang Baik, Jilid 1, Badan Pengawas Obat dan Makanan Republik Industri, Jakarta.