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"[Berdasarkan Peraturan Menteri Kesehatan Republik Indonesia Nomor 1799 Menkes Per XII 2010 proses pembuatan obat dan atau bahan obat hanya dapat dilakukan oleh Industri Farmasi yakni badan usaha yang memiliki izin dari Menteri Kesehatan untuk melakukan kegiatan pembuatan obat atau bahan obat Pada pelaksanaannya industri farmasi harus menerapkan Cara Pembuatan Obat yang Baik CPOB yang bertujuan untuk menjamin obat dibuat secara konsisten memenuhi persyaratan yang ditetapkan dan sesuai dengan tujuan penggunaannya CPOB terdiri atas 12 pilar yang CPOB mencakup seluruh aspek produksi dan pengendalian mutu Pada pembuatan obat pengendalian secara menyeluruh merupakan hal yang sangat esensial untuk menjamin bahwa konsumen menerima obat yang bermutu tinggi Praktek Kerja Profesi Apoteker yang dilaksanakan di PT Gratia Husada Farma HUFA telah memberikan pemahaman bahwa Apoteker dapat berperan penting di industri farmasi yakni dalam hal manajemen teknis saat pelaksanaan produksi dan pengawasan Selain itu apoteker juga dapat berperan dalam pengembangan produk perencanaan produksi serta penyimpanan barang Kegiatan PKPA ini diharapkan dapat meluluskan calon Apoteker yang berkualitas dan berdaya saing tinggi sehingga dapat menerapkan current Good Manufacturing Practice cGMP untuk menghasilkan produk yang memenuhi syarat Quality Safety dan Efficacy QSE ;Based on the Regulation of the Minister of Health of the Republic of Indonesia Number 1799 Menkes Per XII 2010 the manufacturing process of drugs and or drug ingredients only be carried out by the Pharmaceutical Industry the business entity that has a license from the Minister of Health to conduct the manufacture of drugs or drug ingredients In practice the pharmaceutical industry must implement the Good Manufacturing Practice GMP which aims to ensure the drugs are made consistently meet the requirements set and in accordance with the intended use GMP consists of 12 pillars that covers all aspects of production and quality control In the manufacture of drugs overall control is very essential to ensure that consumers receive high quality drugs Apothecary Profession Profession PKPA conducted at PT Gratia Husada Farma HUFA has given the understanding that pharmacists can play an important role in the pharmaceutical industry in terms of management current technical production implementation and supervision In addition pharmacists can also play a role in product development production planning as well as the storage of goods PKPA activity is expected to pass Pharmacists qualified candidates and competitive so as to apply the current Good Manufacturing Practice cGMP to produce products that meet the requirements of Quality Safety and Efficacy QSE ;Based on the Regulation of the Minister of Health of the Republic of Indonesia Number 1799 Menkes Per XII 2010 the manufacturing process of drugs and or drug ingredients only be carried out by the Pharmaceutical Industry the business entity that has a license from the Minister of Health to conduct the manufacture of drugs or drug ingredients In practice the pharmaceutical industry must implement the Good Manufacturing Practice GMP which aims to ensure the drugs are made consistently meet the requirements set and in accordance with the intended use GMP consists of 12 pillars that covers all aspects of production and quality control In the manufacture of drugs overall control is very essential to ensure that consumers receive high quality drugs Apothecary Profession Profession PKPA conducted at PT Gratia Husada Farma HUFA has given the understanding that pharmacists can play an important role in the pharmaceutical industry in terms of management current technical production implementation and supervision In addition pharmacists can also play a role in product development production planning as well as the storage of goods PKPA activity is expected to pass Pharmacists qualified candidates and competitive so as to apply the current Good Manufacturing Practice cGMP to produce products that meet the requirements of Quality Safety and Efficacy QSE , Based on the Regulation of the Minister of Health of the Republic of Indonesia Number 1799 Menkes Per XII 2010 the manufacturing process of drugs and or drug ingredients only be carried out by the Pharmaceutical Industry the business entity that has a license from the Minister of Health to conduct the manufacture of drugs or drug ingredients In practice the pharmaceutical industry must implement the Good Manufacturing Practice GMP which aims to ensure the drugs are made consistently meet the requirements set and in accordance with the intended use GMP consists of 12 pillars that covers all aspects of production and quality control In the manufacture of drugs overall control is very essential to ensure that consumers receive high quality drugs Apothecary Profession Profession PKPA conducted at PT Gratia Husada Farma HUFA has given the understanding that pharmacists can play an important role in the pharmaceutical industry in terms of management current technical production implementation and supervision In addition pharmacists can also play a role in product development production planning as well as the storage of goods PKPA activity is expected to pass Pharmacists qualified candidates and competitive so as to apply the current Good Manufacturing Practice cGMP to produce products that meet the requirements of Quality Safety and Efficacy QSE ]"

"ABSTRAKPerkembangan dunia kesehatan terutama obat semakin berkembang seiring berjalannya waktu. Harapan masyarakat terhadap kualitas dan keamanan obat juga menjadi lebih tinggi. Industri farmasi memiliki peran dan tanggung jawab terbesar terkait efikasi, keamanan, kualitas dan mutu obat. Dalam penerapan CPOB di industri farmasi, apoteker memegang peran yang penting terutama dalam tugas produksi, pengawasan mutu dan pemastian mutu yang harus dipimpin oleh seorang apoteker. Oleh sebab itu mahasiswa calon apoteker harus berkompeten serta menguasai pengetahuan dan keterampilan yang baik untuk dapat menerapkan CPOB di dalam industri farmasi. Pengetahuan yang didapat mahasiswa selama praktek kerja profesi PT Gratia Husada Farma terkait pekerjaan kefarmasian di industri farmasi, seperti memahami pengembangan obat baru atau trial dan metode pengujiannya, mengikuti alur penerimaan, pengeluaran dan penyimpanan bahan awal dan produk jadi, alur proses produksi obat dan manajemennya, sistem penunjang, dan pengawasan serta penjaminan mutu.

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ABSTRACTThe development of health care and technology, especially drugs, has grown over time. Public expectations of drug quality and safety are also higher. The pharmaceutical industry has the greatest roles and responsibilities related to the efficacy, safety and quality of the drug. In the application of GMP in the pharmaceutical industry, pharmacists have an important role especially in the task of production, quality control and quality assurance that must be led by a pharmacist. Therefore, pharmacist students must be competent and have good knowledge and skills to do the GMP in the pharmaceutical industry. Knowledge gained by student during the professional practice in PT Gratia Husada Farma Semarang is all related to pharmaceutical practice in the pharmaceutical industry, such as understanding the development of new drugs or trials and test methods, knowing the flow of acceptance and storage of raw materials and finished products, the flow of the drug production process and its management, the support systems, the quality control and quality assurance"