Pharmaceutical Industry

Subject Code : SFA-655

module description
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Module Name Pharmaceutical Industry
Module Level, if applicable 4th year Types of teaching and learning Teaching discussion and project development
Code, if applicable SFA-655 Class size 50 – 60
Semester 7th semester Attendance time (hours per week per semester) 2h
Person responsible for the module Dr. apt. Siti Zahliyatul Munawiroh Forms of active participation Discussion
Lecturer(s) Dr. apt. Siti Zahliyatul Munawiroh

Prof. Dr. apt. Yandi Syukri, MSc.

apt. Bambang H. Nugroho, MSc.

apt. Oktavia Indrati, MSc.

 Workload Lecture: 2 (hour) x 14 (meeting) = 28

Preparation and follow up 4 (hour) x 14 (self-learning) = 56
Language English- Indonesia Total workload 84 hours
Relation to curriculum Compulsory course 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 –
Study and examination requirements and forms of examination  Midterm and final term, project assignment and presentation

By the end of this course students should be able to:

  • Apply an attitude of responsibility, dedication, togetherness and discipline based on sincerity, honesty and integrity in making pharmaceutical preparations carefully and thoroughly.
  • Comprehend the theory of Good Manufacturing Practice (GMP) including traditional medicine and cosmetics.
  • Comprehend the design, construction, support facilities and functions of existing equipment in the pharmaceutical industry and their qualifications.
  • Comprehend validation and qualifications in the pharmaceutical industry.
  • Able to know the aspects of pharmaceutical halal products

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 and as well as professional and ethical in leadership and management in the pharmaceutical industry.

Blended Learning

  • 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.
  • Anonim, 2013, Petunjuk Operasional Penerapan Pedoman Cara Pembuatan Obat Yang Baik, Jilid 1, Badan Pengawas Obat dan Makanan Republik Industri, Jakarta.