• SIDRA UROOJ
• Iffath rizwana

ABSTRACT 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.

Keyword: Quality control, Raw material, Finished product, Purity, Pharmacopeia

"REVIEW ARTICLE ON PHARMACEUTICAL ANALYSIS OF TABLETS ACCORDING TO STANDARD PHARMACOPEIAS", International Journal of Emerging Technologies and Innovative Research (www.jetir.org), ISSN:2349-5162, Vol.8, Issue 9, page no.d474-d484, September-2021, Available :http://www.jetir.org/papers/JETIR2109353.pdf

"REVIEW ARTICLE ON PHARMACEUTICAL ANALYSIS OF TABLETS ACCORDING TO STANDARD PHARMACOPEIAS", International Journal of Emerging Technologies and Innovative Research (www.jetir.org | UGC and issn Approved), ISSN:2349-5162, Vol.8, Issue 9, page no. ppd474-d484, September-2021, Available at : http://www.jetir.org/papers/JETIR2109353.pdf