Laporan praktek kerja profesi apoteker di PT Aventis Pharma Jl Jend A Yani Pulomas Jakarta periode 5 Maret 30 April 2014 = Apothecary internship report at PT Aventis Pharma Jl Jend A Yani Pulomas Jakarta period March 5th April 30th 2014
Yosiepin Mulyadi;
Yeni Suciani, supervisor; Maggadani, Baitha Palanggatan, supervisor; Mahdi Jufri, examiner; Rusmala Dewi, examiner; Rusmala Dewi, examiner
(Fakultas Farmasi Universitas Indonesia, 2014)
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| [Nama Yosiepin Mulyadi S Farm Program Studi Profesi Apoteker ndash Fakultas Farmasi UIJudul Laporan Praktek Kerja Profesi Apoteker di PT Aventis Pharma Jl Jend A Yani Pulomas Jakarta Periode 5 Maret ndash 30 April 2014 Industri farmasi erat kaitannya dengan kesehatan manusia dalam rangka perwujudan kesehatan nasional Industri farmasi dikontrol dan diawasi dengan ketat oleh Pemerintah dan Badan POM baik ditinjau dari segi perizinan produksi peredaran maupun kualitas obat yang diedarkan Pada pembuatan obat pengendalian menyeluruh sangat esensial untuk menjamin bahwa konsumen menerima obat yang bermutu tinggi maka Pemerintah mengeluarkan ketentuan dan persyaratan yang harus diterapkan dan dilaksanakan oleh setiap industri farmasi yaitu Cara Pembuatan Obat yang Baik CPOB CPOB menyangkut keseluruhan aspek produksi mulai dari manajemen mutu personalia bangunan dan fasilitas peralatan sanitasi dan higiene produksi pengawasan mutu inspeksi diri audit mutu serta audit dan persetujuan pemasok penanganan keluhan terhadap produk dan penarikan kembali produk dokumentasi pembuatan dan analisis berdasarkan kontrak serta kualifikasi dan validasi Semua industri farmasi harus menerapkan CPOB dalam seluruh aspek dan rangkaian kegiatan pembuatan obat Apoteker mempunyai peranan dan tanggung jawab penting untuk menerapkan aspek aspek yang tercantum dalam CPOB tersebut antara lain sebagai penanggung jawab produksi penanggung jawab pengawasan mutu dan penanggung jawab pemastian manajemen mutu ;ABSTRACT Name Yosiepin Mulyadi S Farm Study Program Apothecary ndash Faculty of Pharmacy UIJudul Apothecary Internship Report at PT Aventis Pharma Jl Jend A Yani Pulomas Jakarta Period March 5th ndash April 30th 2014 The pharmaceutical industry is closely related to human health in the framework of realization of national health The pharmaceutical industry is controlled and closely monitored by the Government and POM both in terms of licensing production distribution and quality of medicines in circulation In the manufacture of drugs a thorough control is essential to ensure that consumers receive high quality drugs the government issued terms and conditions that must be applied and implemented by each of the pharmaceutical industry is the Good Manufacturing Practice GMP GMP involves all aspects of production ranging from quality management personnel premises and facilities equipment sanitation and hygiene production quality control inspection and audit quality itself the handling of complaints against drugs drug recalls and drug handling returns documentation manufacturing and analysis based on the contract and the qualification and validation All the pharmaceutical industry must implement GMP in all aspects of drug manufacturing and circuit events Pharmacists have an important role and responsibility for implementing those aspects listed in the GMP among others as the responsible production responsible for oversight and quality assurance ;ABSTRACT Name Yosiepin Mulyadi S Farm Study Program Apothecary ndash Faculty of Pharmacy UIJudul Apothecary Internship Report at PT Aventis Pharma Jl Jend A Yani Pulomas Jakarta Period March 5th ndash April 30th 2014 The pharmaceutical industry is closely related to human health in the framework of realization of national health The pharmaceutical industry is controlled and closely monitored by the Government and POM both in terms of licensing production distribution and quality of medicines in circulation In the manufacture of drugs a thorough control is essential to ensure that consumers receive high quality drugs the government issued terms and conditions that must be applied and implemented by each of the pharmaceutical industry is the Good Manufacturing Practice GMP GMP involves all aspects of production ranging from quality management personnel premises and facilities equipment sanitation and hygiene production quality control inspection and audit quality itself the handling of complaints against drugs drug recalls and drug handling returns documentation manufacturing and analysis based on the contract and the qualification and validation All the pharmaceutical industry must implement GMP in all aspects of drug manufacturing and circuit events Pharmacists have an important role and responsibility for implementing those aspects listed in the GMP among others as the responsible production responsible for oversight and quality assurance , ABSTRACT Name Yosiepin Mulyadi S Farm Study Program Apothecary ndash Faculty of Pharmacy UIJudul Apothecary Internship Report at PT Aventis Pharma Jl Jend A Yani Pulomas Jakarta Period March 5th ndash April 30th 2014 The pharmaceutical industry is closely related to human health in the framework of realization of national health The pharmaceutical industry is controlled and closely monitored by the Government and POM both in terms of licensing production distribution and quality of medicines in circulation In the manufacture of drugs a thorough control is essential to ensure that consumers receive high quality drugs the government issued terms and conditions that must be applied and implemented by each of the pharmaceutical industry is the Good Manufacturing Practice GMP GMP involves all aspects of production ranging from quality management personnel premises and facilities equipment sanitation and hygiene production quality control inspection and audit quality itself the handling of complaints against drugs drug recalls and drug handling returns documentation manufacturing and analysis based on the contract and the qualification and validation All the pharmaceutical industry must implement GMP in all aspects of drug manufacturing and circuit events Pharmacists have an important role and responsibility for implementing those aspects listed in the GMP among others as the responsible production responsible for oversight and quality assurance ] |
 PR-Yosiepin Mulyadi1.pdf :: Unduh
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| No. Panggil : | PR-Pdf |
| Entri utama-Nama orang : | |
| Entri tambahan-Nama orang : | |
| Entri tambahan-Nama badan : | |
| Subjek : | |
| Penerbitan : | Depok: Fakultas Farmasi Universitas Indonesia, 2014 |
| Program Studi : |
| Bahasa : | ind |
| Sumber Pengatalogan : | LibUI ind rda |
| Tipe Konten : | text |
| Tipe Media : | computer |
| Tipe Carrier : | online resource |
| Deskripsi Fisik : | xv, 131 pages : illustration ; appendix |
| Naskah Ringkas : | |
| Lembaga Pemilik : | Universitas Indonesia |
| Lokasi : | Perpustakaan UI, Lantai 3 |
| No. Panggil | No. Barkod | Ketersediaan |
|---|---|---|
| PR-Pdf | 16-22-05612814 | TERSEDIA |
| Ulasan: |
| Tidak ada ulasan pada koleksi ini: 20390785 |
