The evolution and impact of manufacturing execution systems in pharmaceutical manufacturing

This article examines the evolution and impact of Manufacturing Execution Systems (MES) in the pharmaceutical manufacturing sector. It investigates how these comprehensive software solutions bridge the gap between enterprise planning systems and production floors, providing real-time monitoring capabilities and enhancing regulatory compliance. The article explores the core functions and key components of pharmaceutical MES platforms, identifies the primary factors driving adoption, discusses implementation challenges, and presents an outlook on emerging trends that are beginning to reshape the landscape. By addressing regulatory compliance, operational efficiency, and product quality concerns, MES has transformed from a simple tracking tool to an essential component of digital transformation in pharmaceutical operations, with a practical perspective on how manufacturers with traditional systems can prepare for future technological advancements through incremental approaches.

Authors

Publication Details

Journal
World Journal of Advanced Research and Reviews
Published
2025-04-29
DOI
https://doi.org/10.30574/wjarr.2025.26.1.1389
Citations
1
Primary Topic
Quality and Supply Management
Type
article
Field-Weighted Citation Impact
2.28
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article

The evolution and impact of manufacturing execution systems in pharmaceutical manufacturing

Sarita Santosh Dhage
1 citations
World Journal of Advanced Research and Reviews
Quality and Supply Management
2.28
article

The evolution and impact of manufacturing execution systems in pharmaceutical manufacturing

Sarita Santosh Dhage
article en
1 citations

Abstract

This article examines the evolution and impact of Manufacturing Execution Systems (MES) in the pharmaceutical manufacturing sector. It investigates how these comprehensive software solutions bridge the gap between enterprise planning systems and production floors, providing real-time monitoring capabilities and enhancing regulatory compliance. The article explores the core functions and key components of pharmaceutical MES platforms, identifies the primary factors driving adoption, discusses implementation challenges, and presents an outlook on emerging trends that are beginning to reshape the landscape. By addressing regulatory compliance, operational efficiency, and product quality concerns, MES has transformed from a simple tracking tool to an essential component of digital transformation in pharmaceutical operations, with a practical perspective on how manufacturers with traditional systems can prepare for future technological advancements through incremental approaches.

World Journal of Advanced Research and ReviewsVol. 26(1)
Openalex Percentile: Top 13%
Quality and Supply Management
2.28
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The evolution and impact of manufacturing execution systems in pharmaceutical manufacturing — Sarita Santosh Dhage · World Journal of Advanced Research and Reviews (2025) | TGRS Research Map | TGRS