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Abstrak :
ABSTRAK Untuk bisa mewujudkan misi dan objektifnya, setiap organisasi memerlukan strategi. Strategi dirumuskan dengan Manajemen Strategi. Manajemen Strategi memiliki empat elemen dasar yaitu : analisa situasi, formulasi strategi, implementasi strategi dan evaluasi serta kontrol. Penelitian ini hanya fokus pada dua elemen pertama yaitu analisa situasi dan formulasi strategi. Metode analisa situasi dan strategi yang banyak dijelaskan dalam berbagai literatur cenderung untuk industri manufaktur, Pekerjaan jasa memiliki karakteristik unik yang membedakannya dari pekerjaan manufaktur seperti : intangabilitiy, inseparability, perishability, variability, ownership dan consumer as a participant in the service process. Jika perbedaan ini diabaikan maka dapat terjadi kesalahan dalam menangani pekerjaan jasa. Pada kesempatan ini, telah dibuat metode analisa situasi dan formulasi strategi khusus untuk industri jasa. Metode ini dikembangkan dari metode yang sudah ada dengan memasukkan karakteristik unik pekerjaan jasa padanya, Akibatnya adalah terjadi perubahan pada beberapa bagian dari metode yang ada. Karakter intangability memiliki implikasi pada industry environment yaitu dengan perlunya penambahan elemen baru ' Pengakuan'. Elemen baru ini juga ditambahkan pada Basic Competitive Forces. Karakter inseparability memiliki implikasi pada value chain, yaitu fungsi outbond logistic menjadi tidak diperlukan, serta fungsi produksi dan fungsi marketing disatukan. Akhirnya, pada kesempatan ini dibuat Strategy Formulator, yaitu berupa satu paket pertanyaan-pertanyaan dan arahan-arahan yang akan menghantarkan pengguna merumuskan strategi yang sesuai bagi organisasi jasanya. Strategy formulator ini telah dicobakan pada suatu industri jasa, tempat penulis bekerja yaitu UPT XYZ.

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ABSTRACT Strategy is needed by an organization to accomplish its mission and objectives. The strategy has to be formulated by Strategic Management. Strategic Management consist of four basic elements, that are : situation analysis (environmental scanning), strategy formulation, strategy implementation and evaluation/control. This research was focused on the first two elements, i.e situation analysis and strategy formulation. Situation analysis and strategy formulation method which is explained in many references is more suitable for manufacturing or processing industry. Services sector has a number of distinctive characteristics which differentiate them from manufacturing, such as : intangability, inseparability, perishability, variability, ownership and consumer as participant in the service process. ignoring the differences will result in failure in managing service organizations. By this research, a method for situation analysis and strategy formulation specifically for service sector had been created. This method was developed from the already presence method which is good for manufacturing, by introducing the distinctive characteristics of service sector to the method. It had consequences of change in the already presence method. The intangabilily character had implication on industry environment that need new additional element Pengakuan=Registered'. This new element is also added into Basic Competitive Forces. The inseparability character had implication on value chain analysis, that is the outbond logistic function is not needed anymore, and production function is united with marketing function. Finally, by this research had been created a Strategy Formulator that is a package of questions and directions which will drive the user easily to formulate strategy for its service organization. This Strategy Formulator had been tested on a service organization, UPT XYZ, where researcher is working.

Abstrak :
Praktek kerja profesi di PT. Novell Pharmaceutical Laboratories Periode Bulan Januari ndash; Februari Tahun 2018 bertujuan untuk memahami peran, tugas, dan tanggung jawab apoteker di industri farmasi; memiliki wawasan, pengetahuan, keterampilan, dan pengalaman praktis untuk melakukan pekerjaan kefarmasian di industri farmasi; serta memiliki gambaran nyata tentang permasalahan pekerjaan kefarmasian di industri farmasi, Praktek kerja profesi ini dilaksanakan selama delapan minggu dengan tugas khusus yaitu ldquo;Validasi Metode Analisis Kadar pada Kapsul X menggunakan Kromatografi Cair Kinerja Tinggi rdquo;. Tujuan dari tugas khusus ini adalah untuk mendapatkan metode analisis kadar pada kapsul X yang tervalidasi dalam rangka pembuatan bukti terdokumentasi yang mempunyai jaminan tinggi bahwa metode analisis kadar pada kapsul X dapat dilakukan secara konsisten serta memberikan hasil yang memenuhi spesifikasi yang telah ditetapkan. Secara umum, PT. Novell Pharmaceutical Laboratories telah menerapkan aspek Cara Pembuatan Obat yang Baik CPOB dengan baik dan benar. ......Internship at PT. Novell Pharmaceutical Laboratories Period January - February 2018 aims to understand the duties and responsibilities of pharmacists in the pharmaceutical industry; have the insight, knowledges, skills and practical experiences to undertake pharmaceutical works in pharmaceutical industry; and also have the insight of pharmaceutical practice issues in pharmaceutical industry. This internship was conducted for eight weeks with special assignment ldquo;Method of Analysis Validation for Assay of X Capsule by High Performance Liquid Chromatography rdquo;. The purpose of this special assignment is to create highly guaranteed documented evidence which proves that method of analysis for assay of X Capsule is conducted consistently and produces responses which conforms to the determined specifications. In general, PT. Novell Pharmaceutical Laboratories has applied all aspects of Good Pharmaceutical Practices GMP well and correctly.

Abstrak :
Apoteker dituntut untuk memiliki keahlian dan kewenangan dalam melaksanakan pekerjaan kefarmasian di industri farmasi. Oleh karena itu, diperlukan adanya praktik kerja profesi sehingga calon apoteker mempunyai pemahaman yang lebih mendalam tentang peran dan tanggung jawab Apoteker beserta penerapan CPOB di industri farmasi. Praktik kerja profesi di PT Novell Pharmaceutical bertujuan untuk menambah wawasan, pengetahuan, keterampilan, dan pengalaman praktis untuk melakukan pekerjaan kefarmasian di industri farmasi. Tugas khusus yang diberikan yaitu berjudul ldquo;Validasi Metode Analisis Senyawa Sejenis C pada Kapsul Y 75 mg dan 150 mg menggunakan Kromatografi Cair Kinerja Tinggi rdquo;. Tujuan dari pelaksanaan tugas khusus adalah untuk membuktikan bahwa hasil validasi metode analisis pengotor C pada kapsul Y 75 mg dan 150 mg dapat memberikan hasil yang konsisten dan memenuhi spesifikasi yang telah ditetapkan. Selain itu, analisis pengotor C pada kapsul Y membuktikan bahwa terdapat senyawa polar yang terelusi sebelum zat Y. Secara umum, PT Novell Pharmaceutical Laboratories telah menerapkan 12 aspek CPOB dengan baik dan benar. Penulis mampu memahami peran dan tanggung jawab apoteker dalam industri farmasi dan mendapatkan wawasan, keterampilan dan pengalaman praktis, terutama dalam pengembangan metode analisis.

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Pharmacists must have the expertise and authority to perform pharmaceutical practices in pharmaceutical industry. Therefore, internship in pharmaceutical industry allows pharmacist candidates have a deeper understanding of the duties and responsibilities of pharmacists as well as the application of Good Manufacturing Practices GMP in the pharmaceutical industry. Internship at PT Novell Pharmaceutical Laboratories aims to add insight, knowledge, skills, and practical experience to undertake pharmaceutical practices in the pharmaceutical industry. The special assignment given is ldquo;Method of Analysis Validation for Related Substances Impurity C of Y 75 mg and 150 mg Capsules Using High Performance Liquid Chromatography rdquo;. The purpose of this special assignment is to prove that method of analysis for related substances Impurity C of Y 75 mg and 150 mg capsules is conducted consistently and produces responses which conform to the determined specifications. In addition, analysis of related substances Impurity C in Y capsules also prove that there are polar compounds eluting before Y substance. In general, PT Novell Pharmaceutical Laboratories has applied 12 aspects of GMP well and correctly. The author is able to understand the roles and responsibilities of pharmacists in the pharmaceutical industry and gain insight, skills and practical experience, especially in analytical method development.

Abstrak :
Penetapan kadar zat aktif dipersyaratkan pada produk jadi farmasi berupa tablet untuk memastikan kesesuaian produk dengan spesifikasi yang diinginkan sebelum produk diluluskan dan dipasarkan. Melihat pentingnya pengujian tersebut, maka metode analisis yang digunakan dalam pengujiantersebut harus dipastikan dapat memberikan hasil yang spesifik, akurat, dan presisi untuk zat aktif yang diinginkan sehingga reliabilitas terhadap hasil yang diperoleh dapat meningkat. Oleh karena itu, sebelum metode analisis tersebut digunakan dalam pengujian, perlu dilakukan validasi atau verifikasi terlebih dahulu (Badan Pengawas Obat dan Makanan, 2018). Parameter yang perlu diujikan dalam validasi metode analisis mencakup akurasi, presisi, spesifisitas, batas deteksi, batas kuantitasi, linieritas, dan rentang. Oleh karena itu, dalam laporan tugas khusus ini dipaparkan parameter validasi metode analisis dan contoh protokol validasi metode analisis penetapan kadar tablet DXX 0,075 mg.Metode analisis yang digunakan didasarkan pada metode yang tertera pada monografi obat dalam British Pharmacopoeia dengan adanya sedikit modifikasi sehingga dalam hal ini dilakukan validasi terhadap metode analisis tersebut. ......Determination of the active substance content is required for finished pharmaceutical products in the form of tablets to ensure product conformity with the desired specifications before the product is released and marketed. Seeing the importance of the test, the analytical method used in the test must be ensured to provide specific, accurate, and precise results for the desired active substance so that the reliability of the results obtained can be increased. Therefore, before the analytical method is used in testing, it is necessary to carry out validation or verification first (Food and Drug Supervisory Agency, 2018). Parameters that need to be tested in the validation of analytical methods include accuracy, precision, specificity, detection limit, quantitation limit, linearity, and range. Therefore, in this special assignment report, the validation parameters of the analytical method and an example of the validation protocol for the analytical method of assaying the 0.075 mg tablet of DXX assay are presented. The analytical method used is based on the method listed in the drug monograph in the British Pharmacopoeia with slight modifications so that in this case validation of the analytical method is carried out.

Abstrak :
The underlying principles invented and developed by Dr. Genichi Taguchi (1924 - 2012), for the design of experiments or simulation calculations in multi-parameter systems, are today known as Taguchi Method. Due to the great success, it was extended to many other areas. The book explains the basics of this method in as much detail as necessary and as simply and graphically as possible. The author shows how broad the current application spectrum is and for which different tasks it can be used. The application examples range from optimizing a fermentation process in biotechnology to minimizing costs in mechanical production and maintaining and improving competitiveness in industrial production. The processes described are ideally suited to finding reliable and precise solutions for a wide variety of problems relatively quickly. A real competitive advantage not only in research but also for companies that want to remain competitive in international business competition.

Abstrak :
Jumlah stok akhir seluruh obat di Instalasi Farmasi RS PMI Bogor disetiap bulannya selalu dinilai tinggi, meskipun perencanaan perbekalan sudah dilaksanakan sesuai dengan system dan prosedur yang telah diterapkan. Tujuan Penelitian ini berupaya mendapatkan informasi tentang system perencanaan kebutuhan obat dan mengidentifikasi penggolongan obat berdasarkan analisis ABC serta mampu melakukan perhitungan perkiraan perencanaan dengan menggunakan metode konsumsi. Penelitian dilakukan melalui metode kualitatif. Hasil dari penelitian ini menunjukkan bahwa stok akhir dari obat tidak stabil ada yang jumlahnya tinggi bahkan ada yang berjumlah 0, dan perencanaan tidak detail untuk peritem obat karena tidak adanya analisis penggolongan obat secara ABC. Hal ini disebabkan karena terlalu banyaknya jumlah item obat yang mencapai 2740 item di Instalasi Farmasi disertai dengan tidak stabilnya jumlah pemakaian disetiap bulannya. Belum pernah dilakukannya penggolongan obat secara pareto mempersulit pula dalam melakukan prioritas perencanaan untuk detail obat. Akibatnya stok awal obat sering kali untuk beberapa obat kosong tanpa adanya stok pengaman. Bahkan ada beberapa obat stok awal cukup besar dikarenakan stok akhir obat bulan sebelumnya besar. Penelitian ini menyarankan bahwa RS harus merampingkan jumlah item obat dengan minimal melakukan analisis ABC dulu, lalu frekuensi pemesanan dapat di kurangi dari seminggu 2 (dua) kali menjadi seminggu sekali, diharapkan jumlah perencanaan lebih terkontrol dan stok pengaman bisa dimanfaatkan dengan baik. ......The amount of the stock end of the entire drug Pharmacy Installation RS PMI Bogor every month always rated high, even though the supply planning has been carried out in accordance with the system and procedures have been applied. The purpose of this research was trying to obtain information about system planning needs of medicines and identify drug categorization based on analysis of ABC as well as able to do calculations using the method of planning with estimates of consumption. The research was done through qualitative methods. The results of this study indicate that the stock of the drug is not stable there are a high number of even numbered 0, and no detail for planning drug peritem absence of drug classification analysis for ABC. This is because too high number of drug items which reach 2740 items on Pharmaceutical Installations accompanied by the relative number of not discharging every month. Have never done a drug categorization is also undermines the pareto priority planning for details on the drug. As a result the initial stock of the drug often to empty some of the drugs in the absence of a safety stock. There are even some sizable the initial stock of the drug because the stock end of the drug the month before. This research suggests that the HOSPITAL should streamline the number of items of drugs with a minimum conduct analysis for ABC first, then the frequency reservations can be reduce from week 2 (two) times to once a week, it is expected the number of more controlled planning and safety stock can be put to good use.