Dyah Ayu Ratna Yulianti
Abstrak :
Praktek Kerja Profesi PKP di PT Mahakam Beta Farma dilakukan pada tanggal 3 Januari ndash; 28 Februari 2018. Tujuan pelaksanaan PKP untuk memperoleh gambaran dan pengalaman mengenai peran profesi apoteker di industri farmasi, khususnya dalam bidang pemastian mutu. Industri farmasi adalah badan usaha yang memiliki izin dari Menteri Kesehatan untuk melakukan kegiatan pembuatan obat atau bahan obat. Industri farmasi wajib memenuhi persyaratan Cara Pembuatan Obat yang Baik CPOB . Kegiatan yang dilakukan selama PKP antara lain pengenalan secara umum mengenai PT. Mahakam Beta Farma; induksi ke departemen yang berkaitan dengan pekerjaan kefarmasian yaitu Quality Assurance QA , Quality Control QC , Validasi, Research and Development R D , Mechanical and Engineering, Produksi, Custom Clearance and Warehouse, dan Material and Production Planning MPP . PT Mahakam Beta Farma merupakan salah satu industri farmasi yang telah menerapkan pedoman CPOB dalam setiap kegiatan yang dilakukan, baik dalam proses produksi, pengawasan dan pemastian mutu, serta kegiatan lain yang terkait.
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Internship at PT Mahakam Beta Farma held on January 3rd to February 28th 2018. The aim of this internship to obtain an overview and experience of professional role of pharmacists in pharmaceutical industry, particularly in a quality assurance. Pharmaceutical industry is a corporation that has a license from Minister of Health to manufacturing of drugs or drug materials. Pharmaceutical industry is obliged to comply with the requirements of Good Manufacturing Practice for Pharmaceuticals GMP . Activities conducted during internship among other general introduction about PT Mahakam Beta Farma; induction into department which related pharmacy that are Quality Assurance QA , Quality Control QC , Validation, Research and Development R D , Mechanical and Engineering, Production, Custom Clearance and Warehouse, and Material and Production Planning MPP . PT Mahakam Beta Farma is the one of pharmaceutical industry which has implemented the GMP guidelines in each of activities, both in production process, control and quality assurance, and other related activities.
Depok: Fakultas Farmasi Universitas Indonesia, 2018
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