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Six Sigma is a statistical expression that is applied to the quality management system to develop a structure for process improvement. It is used to measure the degree of deviation of a process from precision. Less than 3.4 parts per million (ppm) of faults is the quality indicator for this approach. To accomplish intended outputs and customer satisfaction, this methodology actively links people, processes, and results logically. Motorola created Six Sigma in the 1980s as a tool for improving process quality. Process development, process design/redesign, and process management are the three core elements it focuses on. The DMAIC (Define, Measure, Analyze, Improve, and Control) and DMADV (Define, Measure, Analyze, Improve, and Control) procedures are used to achieve the six sigma aim (Design, Measure, Analyze, and Define & Verify). It features more data analysis capabilities and a stronger financial focus than TQM. Total Quality Management (TQM) and Six Sigma (Six Sigma) are two effective methodologies for continuous improvement that have a shared purpose and base. The variables, methods, concepts, advantages, limitations, and applications of six sigma in the pharmaceutical business are discussed in this article.
"Six Sigma - A Managerial Tool to improve Pharmaceutical Quality", International Journal of Science & Engineering Development Research (www.ijrti.org), ISSN:2455-2631, Vol.7, Issue 8, page no.445 - 456, August-2022, Available :http://www.ijrti.org/papers/IJRTI2208070.pdf
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2456-3315 | IMPACT FACTOR: 8.14 Calculated By Google Scholar| ESTD YEAR: 2016
An International Scholarly Open Access Journal, Peer-Reviewed, Refereed Journal Impact Factor 8.14 Calculate by Google Scholar and Semantic Scholar | AI-Powered Research Tool, Multidisciplinary, Monthly, Multilanguage Journal Indexing in All Major Database & Metadata, Citation Generator