A Review Article on Pharmaceutical Analysis of Pharmaceutical Industry According to Pharmacopoeias

被引:16
作者
Ahmed, Sony [1 ]
Islam, Md Shafiul [2 ]
Ullah, Borkat [2 ,3 ]
Biswas, Saurav Kanti [1 ]
Azad, Md Abdus Samad [2 ]
Hossain, Md Shahadat [2 ]
机构
[1] Beximco Pharmaceut Ltd, Dept Qual Control, Gazipur 1700, Bangladesh
[2] Noakhali Sci & Technol Univ, Dept Appl Chem & Chem Engn, Noakhali 3814, Bangladesh
[3] Virginia Commonwealth Univ, Dept Chem, Richmond, VA 23284 USA
关键词
Quality control; Raw material; Finished product; Purity; Pharmacopeias; LIQUID-CHROMATOGRAPHIC METHOD; HPLC METHOD; IMPURITIES; ACID;
D O I
10.13005/ojc/360101
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The pharmaceutical tablet must meet specific standards to claim it as a standard drug approval. Pharmaceutical industries test the tablets for maintaining their accuracy following different standard parameters such as identity, strength, quality, purity, and stability, etc. For what why, it is essential to control pharmaceutical processes regardless of the issues that may be addressed. Process control includes inspecting raw materials, controlling processes, and targeting for the finished product. That's why it is significant to monitor the effectiveness of the process control. In connection to this, the adaptation of the production process should comply with the specification as needed, which may also include control of equipment and environment. Pharmaceutical products in the process should be checked appropriately for their identity, strength, quality, and purity and the products are approved or rejected by the quality control unit during the manufacturing process. The highlights of this review are to describe quality control testing of pharmaceutical products by using different instruments for the pharmaceutical industry, according to pharmacopeias.
引用
收藏
页码:1 / 10
页数:10
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