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Rangkuti, Muhammad Wildan Shalli
"Praktik Kerja Profesi di PT. Medifarma Laboratories Periode 1 Februari ndash; 31 Maret Tahun 2017 bertujuan untuk mengerti peranan, tugas dan tanggung jawab apoteker di industri farmasi, memiliki wawasan, pengetahuan dan keterampilan, dan pengalaman praktis untuk melakukan pekerjaan kefarmasian di industri farmasi, memahami penerapan CPOB, dan memiliki gambaran nyata tentang permasalahan pekerjaan kefarmasian di industri farmasi. Tugas khusus yang diberikan berjudul Analisis Uji Batas Timbal pada Bahan Baku Eksipien Pewarna yang bertujuan untuk mendapatkan prosedur analisis timbal pada bahan baku eksipien pewarna yang valid.

Internship at PT. Medifarma Laboratories Period 1 February ndash 31 March Year 2017 aims to know and understand pharmacist work and responsibility at Pharmacy Industry, have competence, knowledge, skill, and experience to handle pharmacy work, understand implementation of GMP, and have real illustration about pharmacy work matter at Pharmacy Industry. The internship given a special assignment about Lead Limit Test Analysis for Raw Materials of Color Excipient with aim to get lead analytical valid procedure for raw materials of color excipient. "
2017
PR-Pdf
UI - Tugas Akhir  Universitas Indonesia Library
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Rizky Ariyanti
"ABSTRAK
Praktik Kerja Profesi Apoteker di PT Medifarma Laboratories bertujuan agar mahasiswa profesi apoteker mengetahui dan memahami tugas, peran, dan tanggung jawab apoteker di suatu industri farmasi. Selain itu, kegiatan Praktik Kerja Profesi juga memfasilitasi mahasiswa dalam memahami gambaran nyata permasalahan kefarmasian di industri farmasi, khususnya pada bagian production planning and invertory control PPIC . Tugas khusus yang diberikan berjudul Pemetaan Mesin dan Kapasitas Mesin. Tujuan dari tugas khusus ini adalah untuk mengetahui kesesuain data antara perhitungan kapasitas mesin dengan sistem otomatis yang dibandingkan dengan perhitungan kapasitas mesin secara manual.

ABSTRACT
Internship at PT Medifarma Laboratories aims to make the pharmacist 39 s professional students know and understand the duties, roles and responsibilities of the pharmacist in a pharmaceutical industry. In addition, internship also facilitates students to understand the real picture of pharmaceutical problems in the pharmaceutical industry, especially in the production planning and inventory control PPIC section. Specific assignment given is entitled Machine Matriks and Machine Capacity. The purpose of this particular assignment is to ensure and compare the data of machine capacity between automatic system with manual system. "
Depok: Fakultas Farmasi Universitas Indonesia, 2017
PR-Pdf
UI - Tugas Akhir  Universitas Indonesia Library
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Nabila Ariestiani
"Implementasi dokumentasi merupakan hal yang wajib dilakukan disetiap industri farmasi, termasuk PT. Medifarma Laboratories. PT. Medifarma Laboratories merupakan industri farmasi yang bergerak sebagai toll—manufacturer, yaitu sebagian besar produknya di ekspor ke luar negeri. Hal ini membuat dokumentasi menjadi hal penting dalam memenuhi persyaratan Cara Pembuatan Obat yang Baik (CPOB). Namun PT. Medifarma Laboratories belum memiliki dokumentasi yang baik. Hal ini berkaitan dengan belum adanya lembar kerja mengenai analisis pengembangan produk baru, seperti pada produk Sangobion Capsule Reformulation, sehingga seluruh kegiatan analisis produk tersebut tidak terdokumentasi. Laporan praktik kerja ini bertujuan untuk membuat lembar kerja (worksheet) evaluasi untuk uji analitik dan fisik agar CPOB di PT. Medifarma Laboratories dapat diaplikasikan dengan baik. Kedua lembar kerja dibuat sesuai ketentuan CPOB serta dibuat dengan kolom yang dapat diisi apabila hasil telah disetujui, ditandatangani, dan diberi tanggal oleh pihak yang berwenang. Hal ini sudah sesuai dengan peraturan yang berlaku di PT. Medifarma Laboratories. Lembar kerja yang akan digunakan secara konsisten ini dapat membantu memastikan keamanan dan kualitas produk sehingga memperkecil risiko kesalahan pelaksanaan oleh analis laboratorium.

Implementation of documentation is something that must be done in every pharmaceutical industry, including PT. Medifarma Laboratories. PT. Medifarma Laboratories is a pharmaceutical industry that operates as a toll manufacturer, meaning that most of its products are exported abroad. This makes documentation important in fulfilling the requirements for Good Medicine Manufacturing Practices (CPOB). However PT. Medifarma Laboratories does not yet have good documentation. This is related to the absence of worksheets regarding the analysis of new product development, such as the Sangobion Capsule Reformulation product, so that all product analysis activities are not documented. This work practice report aims to create an evaluation worksheet for analytical and physical tests for CPOB at PT. Medifarma Laboratories can be applied well. Both worksheets are made in accordance with CPOB regulations and are made with columns that can be filled in if the results have been approved, signed and dated by the authorized party. This is in accordance with the regulations in force at PT. Medifarma Laboratories. This worksheet, which will be used consistently, can help ensure product safety and quality, thereby minimizing the risk of implementation errors by laboratory analysts."
Depok: Fakultas Farmasi Universitas ndonesia, 2023
PR-pdf
UI - Tugas Akhir  Universitas Indonesia Library
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Anggun Pramuda Wardhani
"[ABSTRAK
Praktik Kerja Profesi dilaksanakan di PT. Medifarma Laboratories yang
berlangsung pada periode 01 Februari ? 30 Maret 2015. Kegiatan PKP ini
bertujuan agar mahasiswa profesi apoteker dapat melihat langsung kegiatan di
industri farmasi, memperoleh pengetahuan dan wawasan tentang segala aspek
terkait industri farmasi terutama dalam hal penerapan CPOB dan memahami
peran dan tugas apoteker di industri farmasi. Tugas khusus yang diberikan
berkaitan dengan forced degradation studi yang bertujuan untuk mengetahui
kemampuan metode analisis dalam mengukur respon analit dengan adanya
matriks sampel dan cemaran yang spesifik sehingga dapat digunakan sebagai
metode analisa rutin untuk pengujian kadar obat pada sampel stability. ABSTRACT Professional Internship was held at PT. Medifarma Laboratories on February 1st
? March 30th 2015. This Professional Internship is aimed to allow the apothecary
profession students to see directly the activity in the pharmaceutical industry, to
gain knowledge and insight at all aspects related to the pharmaceutical industry
especially in terms of the GMP implementation, and to understand the role and
duties of pharmacist in the pharmaceutical industry. The theme of special
assignment that is given is about Forced Degradation studies with the purpose of
study to determine any various degradant in drug product and to find out stability
of drug product in order to generate ore stable formulations.;Professional Internship was held at PT. Medifarma Laboratories on February 1st
? March 30th 2015. This Professional Internship is aimed to allow the apothecary
profession students to see directly the activity in the pharmaceutical industry, to
gain knowledge and insight at all aspects related to the pharmaceutical industry
especially in terms of the GMP implementation, and to understand the role and
duties of pharmacist in the pharmaceutical industry. The theme of special
assignment that is given is about Forced Degradation studies with the purpose of
study to determine any various degradant in drug product and to find out stability
of drug product in order to generate ore stable formulations.;Professional Internship was held at PT. Medifarma Laboratories on February 1st
? March 30th 2015. This Professional Internship is aimed to allow the apothecary
profession students to see directly the activity in the pharmaceutical industry, to
gain knowledge and insight at all aspects related to the pharmaceutical industry
especially in terms of the GMP implementation, and to understand the role and
duties of pharmacist in the pharmaceutical industry. The theme of special
assignment that is given is about Forced Degradation studies with the purpose of
study to determine any various degradant in drug product and to find out stability
of drug product in order to generate ore stable formulations., Professional Internship was held at PT. Medifarma Laboratories on February 1st
– March 30th 2015. This Professional Internship is aimed to allow the apothecary
profession students to see directly the activity in the pharmaceutical industry, to
gain knowledge and insight at all aspects related to the pharmaceutical industry
especially in terms of the GMP implementation, and to understand the role and
duties of pharmacist in the pharmaceutical industry. The theme of special
assignment that is given is about Forced Degradation studies with the purpose of
study to determine any various degradant in drug product and to find out stability
of drug product in order to generate ore stable formulations.]"
Fakultas Farmasi Universitas Indonesia, 2015
PR-PDF
UI - Tugas Akhir  Universitas Indonesia Library
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Ghaathy Najuda
"Industri farmasi merupakan badan usaha yang memiliki izin untuk melakukan kegiatan pembuatan obat atau bahan obat. Industri harus selalu memenuhi persyaratan Cara Pembuatan Obat yang Baik untuk menjamin bahwa obat yang dihasilkannya bermutu, aman, dan efektif. Kualitas obat yang ditawarkan industri kepada pelanggan haruslah kualitas yang baik dengan harga yang terjangkau dan pelayanan yang baik. Di sisi lain industri memerlukan laba untuk dapat melanjutkan aktivitas bisnis perusahaannya dan bertahan di dalam persaingan. Hal tersebut dapat diperoleh dengan melakukan perbaikan berkelanjutan continuous improvement yang memanfaatkan tools Operational Excellence. Pemanfaatan tools Operational Excellence dipilih sebagai topik tugas khusus. Tugas khusus dilakukan terhadap produk yang paling diminati di pasaran yaitu Tablet Flu Berlapis dan Tablet Multivitamin Salut Gula.

Pharmaceutical industries is a business entity that has permission to perform activities of producing medicines or medicinal materials. The industry has to fulfill the requirements of Good Manufacturing Practice to ensure that the medicines they produce are high quality, safety, and effective. The quality of medicines that industry offers to customers must be good quality with affordable price and good services. On the other hand, industry needs profits to continue its business activities and survive in the competition. This can be achieved by continuous improvement using Operational Excellence tools. The implementation of Operational Excellence tools was chosen as the topic of specific task. Specific task was performed to the products that highly market demand, such as Layered Flu Tablet and Sugar coated Multivitamin Tablet.
"
Depok: Fakultas Farmasi Universitas Indonesia, 2017
PR-pdf
UI - Tugas Akhir  Universitas Indonesia Library
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Subhan Asfari
"ABSTRAK
Industri farmasi merupakan salah satu sarana tempat dilakukan pekerjaan kefarmasian. Praktik kerja profesi yang dilaksanakan di PT Medifarma Laboratories ini, bertujuan agar mahasiswa mendapatkan pengalaman nyata dalam melakukan pekerjaan kefarmasian di industri farmasi. Industri farmasi adalah badan usaha yang memiliki izin untuk melakukan kegiatan pembuatan obat atau bahan obat. Dalam pembuatan obat, industri farmasi harus memenuhi ketentuan Cara Pembuatan Obat yang Baik CPOB agar obat yang dihasilkan aman, berkhasiat dan bermutu. Seluruh aspek CPOB telah diterapkan oleh PT Medifarma Laboratories. Selain itu, PT Medifarma Laboratories juga menerapkan ketentuan GMP dari PIC/s sebagai jaminan tambahan untk keperluan ekspor produk. Seluruh proses produksi dan aspek terkait telah dikendalikan, dan setiap tahapnya telah terdokumentasikan. Salah satu upaya pengendalian dalam proses produksi adalah validasi proses yang menjadi tugas khusus yang diberikan kepada mahasiswa. Validasi proses merupakan usaha untuk membangun bukti terdokumentasi bahwa suatu proses produksi akan senantiasa menghasilkan produk yang memenuhi kriteria yang ditentukan. Validasi ini termasuk dalam validasi konkuren, dilakukan terhadap pada tiga bets tablet suplemen XYZ berturut-turut, dimana tiap bets berukuran 100.000 tablet. Validasi proses telah dilakukan mulai dari tahap wet compounding, dry mixing, compression dan coating. Validasi terhadap proses blistering tablet suplemen XYZ juga telah dilakukan. Dari hasil validasi, disimpulkan bahwa proses produksi tiga bets tablet suplemen XYZ telah tervalidasi.

ABSTRACT
The pharmaceutical industry is one of the places to do the pharmaceutical works. The internship that held at PT Medifarma Laboratories, intended to make students get the real experience in performing the pharmaceutical works in the pharmaceutical industry. The pharmaceutical industry is an entity that has a license to conduct the manufacture of drugs or drug ingredients. In the manufacture of drugs, the pharmaceutical industry must comply Good Manufacturing Practice GMP so that the resulting drug meet the criteria of safe, efficacy and quality. All aspects of GMP has been applied by PT Medifarma Laboratories. In addition, PT Medifarma Laboratories also applying the GMP provisions of PIC s as an additional guarantee for export products. The whole process of production and its related aspects are controlled, and every stage is documented. One of the actions in order to control the production process is validation process that became task given to the student. The validation process is establishing documented evidence to determine that process consistently produce a product meet its predetermined specifications and quality characteristics. Validation that had been done is classified as concurrent validation, and were carried out on three batches of Tablet Supplements XYZ, where the size of each batch were 100.000 tablets. Validation process were started from wet compounding, dry mixing, compression, and coating. Validation of the blistering process Tablets Supplement XYZ had also been performed. The results showed that the production process of three batches of Tablet Supplements XYZ had been validated."
Depok: Fakultas Farmasi Universitas Indonesia, 2017
PR-pdf
UI - Tugas Akhir  Universitas Indonesia Library
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Talogo, Adina Siti Maryam
"ABSTRAK
Praktek Kerja Profesi PKP di industri farmasi dilaksanakan PT Medifarma Laboratories Kegiatan ini berlangsung selama delapan minggu dari tanggal 30 Juni sampai dengan tanggal 24 Agustus 2015 PKP di apotek bertujuan agar mahasiswa apoteker mengerti peranan apoteker tugas dan tanggung jawab apoteker memiliki wawasan pengetahuan keterampilan dan pengalaman praktis untuk melakukan pekerjaan kefarmasian memahami penerapan Cara Pembuatan Obat dengan Baik di Industri Farmasi dan memiliki gambaran nyata tentang permasahalan pekerjaan kefarmasian di Industri Farmasi Sebelum ditempatkan pada masing masing departemen untuk melaksanakan kegiatan PKPA mahasiswa PKPA diberikan pengetahuan berupa gambaran yang meliputi kegiatan dan tugas masing masing departemen yang ada di PT Medifarma Laboratories yaitu Quality Assurance Pemastian Mutu Quality Control Pengawasan Mutu Manufacturing Technology Unit Produksi Engineering HSSE Health Safety Security and Environment dan Logistik Berdasarkan kegiatan PKP yang dilakukan dapat disimpulkan bahwa peran apoteker penting untuk menghasilkan obat obatan yang aman bermutu dan berkhasiat Berdasarkan pengamatan PT Medifarma telah menerapkan seluruh aspek CPOB dengan baik Contoh masalah di PT Medifarma Laboratories adalah target produksi yang sering mengesampingkan standar CPOB baik itu dari urutan validasi personalia sanitasi dan hygiene ABSTRACT Profession Internship n the pharmaceutical industry held by PT Medifarma Laboratories This activity was held for eight weeks from June 30th until August 24th 2015 Profession internship at pharmaceutical industry was intended to make students understand the role of the pharmacist duties and responsibilities of pharmacists has the insight knowledge skills and practical experience to do the job pharmacy understand the implementation of the Good Manufacturing Practice in the Pharmaceutical Industry and have a real picture about the problems of pharmaceutical jobs in the Pharmaceutical Industry Before being placed in each department to carry out the activities PKPA PKPA students are given the knowledge in the form of a picture that includes activities and tasks for each department in the PT Medifarma Laboratories the Quality Assurance Quality assurance Quality Control Quality Control Manufacturing Technology Unit Production Engineering HSSE Health Safety Security and Environment and Logistics Based on PFM activities undertaken it can be concluded that the role of the pharmacist is important to produce medicines that are safe quality and berkhasiat Berdasarkan observations PT Medifarma have implemented all aspects of GMP well Examples of problems in PT Medifarma Laboratories is a frequent target of production of GMP standard rule out either of the order validation personnel sanitation and hygiene ;Profession Internship n the pharmaceutical industry held by PT Medifarma Laboratories This activity was held for eight weeks from June 30th until August 24th 2015 Profession internship at pharmaceutical industry was intended to make students understand the role of the pharmacist duties and responsibilities of pharmacists has the insight knowledge skills and practical experience to do the job pharmacy understand the implementation of the Good Manufacturing Practice in the Pharmaceutical Industry and have a real picture about the problems of pharmaceutical jobs in the Pharmaceutical Industry Before being placed in each department to carry out the activities PKPA PKPA students are given the knowledge in the form of a picture that includes activities and tasks for each department in the PT Medifarma Laboratories the Quality Assurance Quality assurance Quality Control Quality Control Manufacturing Technology Unit Production Engineering HSSE Health Safety Security and Environment and Logistics Based on PFM activities undertaken it can be concluded that the role of the pharmacist is important to produce medicines that are safe quality and berkhasiat Berdasarkan observations PT Medifarma have implemented all aspects of GMP well Examples of problems in PT Medifarma Laboratories is a frequent target of production of GMP standard rule out either of the order validation personnel sanitation and hygiene ;Profession Internship n the pharmaceutical industry held by PT Medifarma Laboratories This activity was held for eight weeks from June 30th until August 24th 2015 Profession internship at pharmaceutical industry was intended to make students understand the role of the pharmacist duties and responsibilities of pharmacists has the insight knowledge skills and practical experience to do the job pharmacy understand the implementation of the Good Manufacturing Practice in the Pharmaceutical Industry and have a real picture about the problems of pharmaceutical jobs in the Pharmaceutical Industry Before being placed in each department to carry out the activities PKPA PKPA students are given the knowledge in the form of a picture that includes activities and tasks for each department in the PT Medifarma Laboratories the Quality Assurance Quality assurance Quality Control Quality Control Manufacturing Technology Unit Production Engineering HSSE Health Safety Security and Environment and Logistics Based on PFM activities undertaken it can be concluded that the role of the pharmacist is important to produce medicines that are safe quality and berkhasiat Berdasarkan observations PT Medifarma have implemented all aspects of GMP well Examples of problems in PT Medifarma Laboratories is a frequent target of production of GMP standard rule out either of the order validation personnel sanitation and hygiene ;Profession Internship n the pharmaceutical industry held by PT Medifarma Laboratories This activity was held for eight weeks from June 30th until August 24th 2015 Profession internship at pharmaceutical industry was intended to make students understand the role of the pharmacist duties and responsibilities of pharmacists has the insight knowledge skills and practical experience to do the job pharmacy understand the implementation of the Good Manufacturing Practice in the Pharmaceutical Industry and have a real picture about the problems of pharmaceutical jobs in the Pharmaceutical Industry Before being placed in each department to carry out the activities PKPA PKPA students are given the knowledge in the form of a picture that includes activities and tasks for each department in the PT Medifarma Laboratories the Quality Assurance Quality assurance Quality Control Quality Control Manufacturing Technology Unit Production Engineering HSSE Health Safety Security and Environment and Logistics Based on PFM activities undertaken it can be concluded that the role of the pharmacist is important to produce medicines that are safe quality and berkhasiat Berdasarkan observations PT Medifarma have implemented all aspects of GMP well Examples of problems in PT Medifarma Laboratories is a frequent target of production of GMP standard rule out either of the order validation personnel sanitation and hygiene "
Fakultas Farmasi Universitas Indonesia, 2016
PR-PDF
UI - Tugas Akhir  Universitas Indonesia Library
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Deni Lastanto
"ABSTRAK
Praktik kerja profesi di PT. Medifarma Laboratories Periode Bulan Agustus-September 2017 bertujuan untuk mengetahui tugas dan tanggung jawab apoteker di industri farmasi dan memahami penerapan Cara Pembuatan Obat yang Baik CPOB di Industi Farmasi. Selain itu calon apoteker juga dapat memiliki gambaran nyata tentang permasalahan pekerjaan kefarmasian di industri farmasi, memiliki wawasan, pengetahuan, keterampilan, dan pengalaman praktis untuk melakukan pekerjaan kefarmasian di industri farmasi. Tugas khusus yang diberikan yaitu berjudul ldquo;Value Stream Mapping Produk Jadi rdquo;. Tujuan dari tugas khusus ini adalah mengidentifikasi waste dan akar penyebab waktu tunggu proses pengiriman produk jadi dan penumpukan produk jadi di secondary packaging, staging area dan warehouse, serta mengusulkan ide continous improvement untuk mengurangi waktu tunggu dan penumpukan produk jadi di secondary packaging, staging area, dan warehouse.

ABSTRACT
Internship at PT. Medifarma Laboratories month period August-September 2017 aims to understand the duties and responsibilities of pharmacists in the pharmaceutical industry and the understanding of the application of good manufacturing practice GMP in the pharmaceutical industry. In addition, the pharmacist candidate can also have the insight, knowledge, skills and practical experience to undertake pharmaceutical work in the pharmaceutical industry. The special assignment given is ldquo;Value Stream Mapping of Finished Goods rdquo;. The purpose of this special assignment is to identify waste and root cause of lead time of finished product delivery and accumulation of finished product in secondary packaging, staging area and warehouse, and propose continous improvement idea to reduce lead time and accumulation of finished product in secondary packaging, staging area and warehouse "
2017
PR-Pdf
UI - Tugas Akhir  Universitas Indonesia Library
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Atvinda Prilya Afista
"ABSTRAK
Praktek Kerja Profesi (PKP) di industri farmasi dilaksanakan di Departemen
Quality Control (QC) PT Medifarma Laboratories. Kegiatan ini berlangsung
selama 2 bulan dari tanggal 1 Juli sampai dengan tanggal 31 Agustus 2015. PKP di
industri bertujuan agar mahasiswa apoteker mengerti peranan, tugas, dan tanggung
jawab Apoteker di Industri Farmasi; memiliki wawasan, pengetahuan,
keterampilan, dan pengalaman praktis untuk melakukan pekerjaan kefarmasian di
Industri Farmasi; memahami penerapan CPOB di Industri Farmasi; memiliki
gambaran nyata tentang permasalahan pekerjaan kefarmasian di Industri Farmasi.
Berdasarkan kegiatan PKP yang dilakukan, dapat disimpulkan bahwa peran
apoteker penting untuk menghasilkan obat-obatan yang aman, bermutu, dan
berkhasiat. Apoteker di Departemen QC bertanggung jawab untuk melakukan
pengawasan mutu terhadap produk yang diproduski dan memastikan bahwa
pengujian yang diperlukan dan relevan telah dilakukan dan bahwa bahan yang
belum diluluskan tidak digunakan serta produk yang belum diluluskan tidak dijual
atau dipasok sebelum mutunya dinilai dan dinyatakan memenuhi syarat. Mahasiswa
apoteker telah berhasil memperoleh gambaran umum dari pelaksanaan pekerjaan
kefarmasian di PT Medifarma., khususnya di bidang QC yaitu melakukan analisis
terhadap bahan awal, produk jadi, inspeksi bahan awal. Dalam melakukan tugasnya
di QC juga mahasiswa apoteker membuat Spreadsheet dan cara memvalidasinya
untuk mendukung analisis dan inspeksi bahan awal. Adanya PKP di PT Medifarma
Laboratories yang telah melaksanakan CPOB dengan baik di semua aspek, peserta
PKP lebih banyak mengetahui dan memahami seperti apa pelaksanaan CPOB
secara real dalam sebuah Industri. Seperti Industri yang lainnya PT Medifarma
Laboratories juga memiliki masalah seperti berpikir bagaimana mengatasi waste
time pada proses maupun para pekerja sehingga suatu proses berlangsung lebih
cepat tetapi tetap menghasilkan hasil yang baik dan dapat dipertanggungjawabkan,
Oleh karena itu, Apoteker harus memiliki wawasan, pengetahuan dan kreatifitas
sehingga dapat mengatasi masalah-masalah tersebut.

ABSTRACT
Profession Internship at pharmaceutical industry was held at Quality Control (QC)
Department of PT Medifarma Laboratories. This activity was held for two month
from July 1
st
until August 31
th
2015. Profession internship at pharmaceutical
industry was intended to make apothecary student understand the role of
pharmacist, have insight into the implementation of pharmaceutical practice,
understand the implementation of Cara Pembuatan Obat yang Baik (CPOB), and
know the issues in pharmaceutical practice in pharmaceutical industry. Based on
the activities, Apothecary at QC Department is responsible for supervising the
quality of the product diproduski and ensure that the necessary and relevant tests
have been conducted and that the materials have not been approved are not used as
well as products that have not been approved are not sold or supplied before the
quality was assessed and found eligible. Apothecary student have obtained insight
into general routine activities in QC Department, those were an analysis of the
starting materials, finished products, inspection of the starting material. In
performing the task in QC department, apothecary student make a spreadsheet and
validate them to support the analysis and inspection of the starting material. PT
Medifarma Laboratories that has implemented the GMP well in all aspects, give
apothecary student more aware and understand what the real implementation of
GMP in an industry. Such as Industrial others, PT Medifarma Laboratories also has
a problem such as find solution how to solve waste time in the process or the
workers, so that a process was faster but still produce good results. Therefore,
pharmacists should have the insight, knowledge and creativity so that can overcome
the problems.
;Profession Internship at pharmaceutical industry was held at Quality Control (QC)
Department of PT Medifarma Laboratories. This activity was held for two month
from July 1
st
until August 31
th
2015. Profession internship at pharmaceutical
industry was intended to make apothecary student understand the role of
pharmacist, have insight into the implementation of pharmaceutical practice,
understand the implementation of Cara Pembuatan Obat yang Baik (CPOB), and
know the issues in pharmaceutical practice in pharmaceutical industry. Based on
the activities, Apothecary at QC Department is responsible for supervising the
quality of the product diproduski and ensure that the necessary and relevant tests
have been conducted and that the materials have not been approved are not used as
well as products that have not been approved are not sold or supplied before the
quality was assessed and found eligible. Apothecary student have obtained insight
into general routine activities in QC Department, those were an analysis of the
starting materials, finished products, inspection of the starting material. In
performing the task in QC department, apothecary student make a spreadsheet and
validate them to support the analysis and inspection of the starting material. PT
Medifarma Laboratories that has implemented the GMP well in all aspects, give
apothecary student more aware and understand what the real implementation of
GMP in an industry. Such as Industrial others, PT Medifarma Laboratories also has
a problem such as find solution how to solve waste time in the process or the
workers, so that a process was faster but still produce good results. Therefore,
pharmacists should have the insight, knowledge and creativity so that can overcome
the problems."
2016
PR-PDF
UI - Tugas Akhir  Universitas Indonesia Library
cover
Rizal Abdullah
"PT Medifarma Laboratories adalah industri farmasi toll manufacturing yang terletak di Indonesia. Sebagai sebuah industri farmasi, perusahaan ini memiliki target produk yang harus dicapai, namun pada kenyataannya seringkali target tersebut tidak tercapai akibat dari munculnya berbagai permasalahan yeng terjadi selama produksi. Sehingga perlu ditemukan solusi yang tepat untuk meningkatkan kapasitas produksi di PT Medifarma Laboratories. Pada tugas khusus ini akan berfokus pada salah satu mesin yang digunakan dalam proses pengemasan primer di PT Medifarma Laboratories yaitu mesin Noack NBP 950. Penelitian ini bertujuan untuk meningkatkan kapasitas produksi dan mengurangi jumlah limbah blister pada proses pengemasan dengan menggunakan mesin Noack NBP 950. Sehingga target hasil akhir produksi dapat dicapai secara cost-efektif. Penyusunan laporan ini dilakukan melalui pengolahan dan analisis data downtime dari logbook primary packaging mesin Noack NBP 950. Hasil penyusunan laporan ini menunjukkan bahwa untuk planned downtime yang sering ditemukan pada mesin Noack NBP 950 adalah penggantian foil dan pvc. Sedangkan untuk unplanned downtime yang sering ditemukan adalah ink jet error/not ready. Untuk meningkatkan kapasitas dan mengurangi jumlah limbah yang dihasilkan mesin Noack NBP 950, diperlukan solusi-solusi diantaranya cleaning die roll, perbaikan atau penggantian vacuum track, dan inspeksi oleh QC. Hasil laporan ini dapat dijadikan sebagai sumber informasi dalam upaya untuk mengurangi jumlah limbah produksi dan meningkatkan kapasitas produksi agar mencapai target yang telah ditetapkan oleh industri farmasi.

PT Medifarma Laboratories is a toll manufacturing pharmaceutical industry located in Indonesia. As a pharmaceutical industry, this company has product targets that must be achieved, but in reality these targets are often not achieved due to the emergence of various problems that occur during production. So it is necessary to find the right solution to increase production capacity at PT Medifarma Laboratories. In this special assignment, we will focus on one of the machines used in the primary packaging process at PT Medifarma Laboratories, namely the Noack NBP 950 machine. This research aims to increase production capacity and reduce the amount of blister waste in the packaging process using the Noack NBP 950 machine. So that the target The final production results can be achieved cost-effectively. This report was prepared by processing and analyzing downtime data from the primary packaging logbook of the Noack NBP 950 machine. The results of preparing this report show that the planned downtime that is often found on the Noack NBP 950 machine is replacing foil and PVC. Meanwhile, unplanned downtime that is often found is ink jet error/not ready. To increase capacity and reduce the amount of waste produced by the Noack NBP 950 machine, solutions are needed including cleaning die rolls, repairing or replacing vacuum tracks, and inspection by QC. The results of this report can be used as a source of information in an effort to reduce the amount of production waste and increase production capacity in order to achieve targets set by the pharmaceutical industry."
Depok: Fakultas Farmasi Universitas Indonesia, 2023
PR-pdf
UI - Tugas Akhir  Universitas Indonesia Library
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