Aim of the present review is to summarize various steps involved in process validation of the oral solid dosage forms in pharmaceutical industries. Oral solid dosage form such as tablets, capsules etc are widely used due to its easy administration and easily available to the market at affordable price. Validation it is an important part of current good manufacturing practice. Process validation is an integral part of GMP as it provides evidence for the quality of drug product. Performing process validation in pharmaceutical industries, will help to design, control and maintain the particular process. The critical process steps such as sifting, mixing, compression etc and critical process parameters such as sieve integrity before and after passing the raw materials, sieve size, mixing time, mixing speed, compression force etc., it is well stated. Process validation establishes evidence and provides high degree of assurance that a particular process will consistently produce a product meeting its predefined specifications.
by Mr. Rajesh Dumpala | Mr. Chirag Patil "A Review on Solid Oral Dosage Forms with an Industrial Perspective for Process Validation"
Published in International Journal of Trend in Scientific Research and Development (ijtsrd), ISSN: 2456-6470, Volume-4 | Issue-6 , October 2020,
URL: https://www.ijtsrd.com/papers/ijtsrd33624.pdf
internationaljournalofscience, openaccessjournalofscience, ugcapprovedjournalsforscience
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