Author(s):
Kalyani K. Gardi, B.P. Chaudhari, V. K. Redasani, Kashish Mulani
Email(s):
Kalyanigardi2003@gmail.com
DOI:
10.52711/2231-5659.2025.00045 
Address:
Kalyani K. Gardi*, B.P. Chaudhari, V. K. Redasani, Kashish Mulani
Yashoda Technical Campus, Faculty of Pharmacy, Wadhe, Satara.
*Corresponding Author
Published In:
Volume - 15,
Issue - 3,
Year - 2025
ABSTRACT:
The introduction of validation and a standard framework for process validation in the Pharmaceutical business are the main topics of this essay. “Validation is documented evidence that provides a high degree of assurance” is the definition of validation. Validation has emerged as a crucial medicinal topics that are acknowledged by industries. Quality assurance techniques must be used to build the quality into the product at every step and not just tested for at the end. Process validation of a process will ensure production of a drug of Reproducible quality. Additionally, process validation emphasizes the need of objective actions and statistical Techniques, as well as knowledge, discrepancy detection, and control, and provides guarantee of consistent quality. Throughout the product’s life cycle.
Cite this article:
Kalyani K. Gardi, B.P. Chaudhari, V. K. Redasani, Kashish Mulani. Pharmaceutical Process Validation. Asian Journal of Research in Pharmaceutical Sciences. 2025; 15(3):309-4. doi: 10.52711/2231-5659.2025.00045
Cite(Electronic):
Kalyani K. Gardi, B.P. Chaudhari, V. K. Redasani, Kashish Mulani. Pharmaceutical Process Validation. Asian Journal of Research in Pharmaceutical Sciences. 2025; 15(3):309-4. doi: 10.52711/2231-5659.2025.00045 Available on: https://ajpsonline.com/AbstractView.aspx?PID=2025-15-3-12
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