Praktek Kerja Profesi Apoteker di Direktorat Bina Produksi dan Distribusi Alat Kesehatan Direktorat Jenderal Bina Kefarmasian dan Alat Kesehatan Kementerian Kesehatan Republik Indonesia bertujuan untuk memahami secara umum struktur organisasi Kementerian Kesehatan dan Direktorat Jenderal Bina Kefarmasian dan Alat Kesehatan Kementerian Kesehatan Republik Indonesia, struktur organisasi, tugas dan fungsi Direktorat Bina Produksi dan Distribusi Alat Kesehatan serta memperoleh wawasan dan pengetahuan mengenai peranan apoteker dalam bidang pelayanan kefarmasian khususnya dalam bidang produksi dan distribusi alat kesehatan dan perbekalan kesehatan rumah tangga. Tugas khusus yang diberikan berjudul Tinjuan ISO 13485 Pedoman Manajemen Mutu Industri Alat Kesehatan terkait Tanggung Jawab dan Manajemen Sumber Daya. Tujuan dari tugas khusus adalah memahami ISO 13485 pedoman manajemen mutu pada industri alat kesehatan serta memahami tanggung jawab manajemen dan manajemen sumber daya dalam ISO 13485 pedoman manajemen mutu alat kesehatan.

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Pharmacists Professional Practice in Directorate of Production and Distribution of Medical Devices Directorate General of Pharmaceutical and Medical Devices of the Republic of Indonesia Ministry of Health aims to understand the general structure of the organization and the Ministry of Health Directorate General of Pharmaceutical and Medical Devices Ministry of Health of the Republic of Indonesia, organizational structure, duty and functions of the Directorate of production and distribution of medical Devices and obtain insight and knowledge about the role of pharmacists in the field of pharmaceutical services especially in the field of production and distribution of medical equipment and home health equipment. Given special assignments titled Improved overview of ISO 13485 Quality Management Guidelines for Medical Devices Industry related Responsibility and Resource Management. The purpose of the special task is to understand the ISO 13485 guidelines for quality management in the medical device industry and understand the responsibilities of management and resource management guidelines in ISO 13485 quality management of medical devices.