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"A collection of test procedures for assessing the identity, purity, and content of medicinal plant materials, including determination of pesticide residues, arsenic and heavy metals. Intended to assist national laboratories engaged in drug quality control, the manual responds to the growing use of medicinal plants, the special quality problems they pose, and the corresponding need for international guidance on reliable methods for quality control. Recommended procedures - whether involving visual inspection or the use of thin-layer chromatography for the qualitative determination of impurities - should also prove useful to the pharmaceutical industry and pharmacists working with these materials."

"Dalam suatu industri farmasi terdapat quality control atau pengawasan mutu terhadap obat yang akan diproduksi. Salah satu aspek yang perlu diawasi adalah bahan baku yang digunakan. Kualitas atau mutu bahan baku menjadi salah satu faktor yang menentukan mutu obat. Raman merupakan salah satu alat yang bisa digunakan untuk menguji identitas bahan dengan metode spektorskopik. Uji identifikasi menggunakan Raman leih efisien, mengurangi biaya, mengurangi lead time dan inventory. Oleh karena itu diperlukan pembuatan metode spektroskopi Raman portabel untuk identifikasi bahan baku di quality control PT Mahakam Beta Farma dan dan membuat data Master List hasil bahan baku yang sudah dibuat metodennya dengan spektroskopi Raman portabel.

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In a pharmaceutical industry there is quality control or quality control of the drugs that will be produced. One aspect that needs to be monitored is the raw materials used. Quality or quality of raw materials is one of the factors that determines the quality of medicines. Raman is a tool that can be used to test the identity of materials using the spectroscopic method. Identification tests using Raman are more efficient, reduce costs, reduce lead time and inventory. Therefore, it is necessary to create a portable Raman spectroscopy method to identify raw materials in quality control at PT Mahakam Beta Farma and create a Master List data on the results of raw materials for which the method has been created using portable Raman spectroscopy."

"BPOM memberikan arahan agar semua industri farmasi memperbarui spesifikasi obat dan bahan baku obat sesuai dengan kompendial terbaru karena ditemukannya cemaran etilen glikol dan dietilen glikol. Arahan tersebut diperoleh dari sosialisasi Badan POM. Pencarian spesifikasi dan metode analisis obat dan bahan obat mengacu pada Farmakope Indonesia (FI) VI dan United States Pharmacopeia (USP) NF 2022, kemudian dilakukan pembandingan antara kedua kompendial. Pengecekan ketersediaan reagent yang digunakan untuk pengujian dilakukan melalui daftar excel reagent yang tersedia di laboratorium. Tugas khusus ini bertujuan untuk menganalisis perbedaan spesifikasi dan metode analisis bahan baku obat pada FI VI dan USP NF 2022 sebagai langkah dalam menentukan metode yang paling baik untuk diimplementasikan serta pengecekan feasibility laboratorium untuk penerapan metode analisis baru.

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BPOM provides directions for all pharmaceutical industries to update drug specifications and drug raw materials in accordance with the latest compendial due to the discovery of ethylene glycol and diethylene glycol contamination. This direction was obtained from the POM Agency's outreach. Search for specifications and analysis methods for drugs and medicinal substances referring to the Indonesian Pharmacopoeia (FI) VI and the United States Pharmacopeia (USP) NF 2022, then a comparison is made between the two compendials. Checking the availability of reagents used for testing is carried out through the Excel list of reagents available in the laboratory. This special assignment aims to analyze the differences in specifications and analytical methods for medicinal raw materials in FI VI and USP NF 2022 as a step in determining the best method to implement as well as checking laboratory feasibility for implementing the new analytical method."