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Quality by design (QbD) is a strategic Process for development and manufacturing. Recently the concept “Quality by Design” gaining much attention among pharmaceutical industries for maintaining quality. The advantage of QbD benefits both the consumer and manufacturer. Some of the QbD elements include quality target product profile (QTPP), CQAs, designing product and manufacturing process, Process parameter and sources of variability. QbD widely promoted by Food and Drug Administration (FDA) and International Conference on Harmonization (ICH). The aim of QbD is to design a quality product and manufacturing process to consistently deliver the intended performance of the product. QbD helps to serve the progressive manufacturing processes, decreases the amount of batch failure, gives more effective control of change and also provide a higher return on investment. In the future, the QbD is going to be accustomed to a far bigger extent. Currently, International Conference on Harmonization is functioning on “ICH- Q13 and ICH- Q14”. This new International Conference on Harmonization tips square measure is expected close to the future.
Keywords:
Quality by Design, Regulatory Guidelines
Cite Article:
"QUALITY BY DESIGN APPROACH: REGULATORY GUIDELINES AND CURRENT STATUS", International Journal for Research Trends and Innovation (www.ijrti.org), ISSN:2455-2631, Vol.7, Issue 6, page no.1029 - 1035, June-2022, Available :http://www.ijrti.org/papers/IJRTI2206165.pdf
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000205262
ISSN:
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