Process Validation as a Critical Enabler in Pharmaceutical Manufacturing

Authors

  • Narendar Kumar Ale Department of Quality Assurance, Acharya & B M Reddy College of Pharmacy, Bengaluru-560107, Karnataka, India

DOI:

https://doi.org/10.66069/ojspub.16560608

Keywords:

process validation, pharmaceutical industry, GMP compliance, product lifecycle, patient safety

Abstract

Process validation is an ongoing programme, essential part of GMP and by aligning process validation operations with the product lifecycle, the pharmaceutical industry ensures that its processes are reliable and consistent over the whole duration of their commercialization. This game-changing practice minimizes risks, reduces costs, and supports continuous improvement, enhancing patient safety and meeting stringent industry standards.

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Published

2026-06-30

How to Cite

Ale, N. K. (2026). Process Validation as a Critical Enabler in Pharmaceutical Manufacturing. Journal of Research in Science and Engineering, 8(6), 33–36. https://doi.org/10.66069/ojspub.16560608

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