Paper Title
Comparative study of in process and finished product Quality control test for IP, BP, and USP For Tablet
Article Identifiers
Authors
Vaishnavi Khanderao Suryawanshi , Kranti Ashok Suryawanshi , Sandesh Ragho Nikam , Dnyaneshwari Suresh Bacchav , Puja.B. Mairal
Keywords
Indian Pharmacopeia, British Pharmacopeia, United, States Pharmacopeia, Tablet Quality control Tests, Quality Control Tests.
Abstract
The present study deals with a brief summary of the evaluation of the quality requirements for finished products quality control and in-process products quality control. Tests with certain common dosage forms according to the Indian Pharmacopeia (IP), British Pharmacopeia (BP), & United States Pharmacopeia (USP).Total quality control relates to the ability to produce a quality products through a number of steps, involving an arrangement to minimize errors at every stage of the production process. To maintain that the finished product conforms to the compendial standards stated in the pharmacopoeias, in-process product testing is performed. The pharmaceutical company works to manufacture high-quality goods, which is achieved by permitting methods for completed product and in-process quality control .There is a significant difference because the final sample used for the finished product testing is actually an example of a significant batch. In the exchange for a value to be compliant with the standards, the pharmacopoeias have defined the prescribed range that the value may stand. The quality standards for pharmaceutical products are specified in various regulatory active ingredients toward the country. Except for a few properties, it was observed that the quality control tests are mostly equivalent. To ensure that the intermediates, packaging materials, and finished pharmaceutical tablets conform with approved specifications or standards for efficacy, safety, and elegance that ensure the consumer that the products Perform consistently and in a manner satisfactory, in-process quality control is a concept that is carried out before, after, and during production covering all steps, including the establishment of specifications, sampling, relevant testing, and analytical clearance. Quality control involves checking products for problems that make it easier for the manufacturer to hold back product releases or conduct potential research to produce optimum pharmaceutical tablets. before released into the market As the comparing pharmacopoeias, an attempt is made to convey the harmonized limitations so that the products should conform with the specification as given in the pharmacopoeias to ensure the quality of pharmaceutical dosage form. This study aims to compare various quality control methods evaluations of medication tablets in accordance with various pharmacopoeia standards.
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How To Cite (APA)
Vaishnavi Khanderao Suryawanshi , Kranti Ashok Suryawanshi , Sandesh Ragho Nikam , Dnyaneshwari Suresh Bacchav , & Puja.B. Mairal (November-2022). Comparative study of in process and finished product Quality control test for IP, BP, and USP For Tablet. INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT, 7(11), b869-b878. https://ijnrd.org/papers/IJNRD2211200.pdf
Issue
Volume 7 Issue 11, November-2022
Pages : b869-b878
Other Publication Details
Paper Reg. ID: IJNRD_184202
Published Paper Id: IJNRD2211200
Downloads: 000121998
Research Area: Pharmacy
Country: Nashik, Maharashtra , India
Published Paper PDF: https://ijnrd.org/papers/IJNRD2211200.pdf
Published Paper URL: https://ijnrd.org/viewpaperforall?paper=IJNRD2211200
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Journal Name: INTERNATIONAL JOURNAL OF NOVEL RESEARCH AND DEVELOPMENT(IJNRD)
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