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.
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Asian Journal of Dental and Health Sciences
Nothing in this world is stable and ever accepted. Change is the requirement of nature for the sake of adaptability. However, the pharmaceutical world is also not far off from this change. Technical advancement in pharma world also leads to the development of new dosages forms. This leads to the replacement of the older dosages forms with the newer once. But for the tablet dosages forms this replacement is substituted with modifications. On the top of it the availability of numerous evaluation parameters provides these new modifications in tablets a clear cut demonstration idea. Tablets are defined as solid unit dosage form of medicaments intended for oral use. They became most popular as they were easy in preparation compared to any other type of dosage forms. But the major drawback exists in its manufacturing. If any minor problem occurs during their manufacturing then the whole batch of the unit should be discarded. It is necessary to avoid any sort of errors during its manufactu.
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Journal of emerging technologies and innovative research
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Research in Pharmacy and Health Sciences
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Particle & Particle Systems Characterization
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International Journal Of Pharmaceutical Sciences
The evaluation of diclofenac potassium tablets involved rigorous testing to ensure quality and efficacy. Tests included hardness assessment to gauge tablet strength, friability testing to determine resistance to action analysis was conducted to ensure uniformity among tablets. This comprehensive evaabrasion, and disintegration tests to assess dissolution properties. Additionally, weight evaluation provides valuable insights into the tablets' physical characteristics, aiding in the assurance of product quality and consistency. This study focuses on the comprehensive evaluation of diclofenac potassium tablets, a crucial step in ensuring their quality and performance. Hardness testing was employed to measure the tablets' resistance to breakage, indicating their strength and durability. Friability assessment gauged the tablets' susceptibility to abrasion, providing insights into their structural integrity during handling and transport. Disintegration tests were conducted to examine the tablets' dissolution properties, crucial for predicting their efficacy upon ingestion. Weight variation analysis ensured uniformity in tablet mass, a critical factor in dosage accuracy and overall product consistency. The findings from these tests collectively contribute to a thorough understanding of the physical attributes of diclofenac potassium tablets. This information is essential for quality control, helping to guarantee that each tablet meets the required standards for hardness, friability, disintegration, and weight variation. As a result, this evaluation provides valuable data for pharmaceutical manufacturers, regulatory authorities, and healthcare professionals, reinforcing the reliability and effectiveness of diclofenac potassium tablets in therapeutic applications.
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A pharmaceutical tablet must satisfy certain standards to claim it to be a quality drug. The main criteria for quality of any drug in dosage form are its safety, potency, efficacy, stability, patient acceptability and regulatory compliance. The quality of a pharmaceutical tablet needs to be designed from the product development stage. At the product design and formulation stage the physical, chemical and biological specifications, to which the product must comply with to fulfill quality requirements, have to determine and the target for quality must be set. In-process quality control (IPQC) tests are strongly related to final product quality because checks performed during production in order to monitor and if necessary to adjust the process to ensure that the product conforms to its specification are the key for good quality pharmaceutical tablets. The purposes of IPQC are to produce a perfect finished product by preventing or eliminating errors at every stage in production. After the manufacturing process is complete finished product quality control (FPQC) tests for pharmaceutical tablets are performed with respect to specification of the pharmacopoeias in order to check that the quality parameters are within acceptance limits or not. The aim of this study is to provide in-process and finished product quality control tests for pharmaceutical tablets according to pharmacopoeias.
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