Author(s):
Nikita Sawant, Bharati P. Caudhari, V. K. Redasani, Saniya Mulla
Email(s):
sawantniki30@gmail.com
DOI:
10.52711/2231-5659.2025.00046 
Address:
Nikita Sawant*, Dr. Bharati P. Caudhari, V. K. Redasani, Saniya Mulla
YSPM’S YTC Faculty of Pharmacy, Satara, Maharashtra, India.
*Corresponding Author
Published In:
Volume - 15,
Issue - 3,
Year - 2025
ABSTRACT:
The Pharmaceutical industries are in a highly regulated environment; hence it requires effective document management processes. Documentation plays a pivotal role in the pharmaceutical industry, serving as a cornerstone for compliance, quality assurance, and overall operational efficiency. This abstract highlight the critical importance of documentation practices within pharmaceutical companies. It explores how meticulous documentation not only ensures adherence to regulatory requirements but also facilitates the maintenance of high-quality standards throughout the product lifecycle. By providing a comprehensive overview of the types of documentation involved, including batch records, standard operating procedures (SOPs), and regulatory filings, this abstract underscore the multifaceted nature of documentation in pharmaceutical manufacturing, research, and development. Ultimately, this abstract emphasizes the indispensable role of documentation in safeguarding public health, fostering innovation, and sustaining the integrity of the pharmaceutical industry.
Cite this article:
Nikita Sawant, Bharati P. Caudhari, V. K. Redasani, Saniya Mulla. Documentation in Pharmaceutical Industry. Asian Journal of Research in Pharmaceutical Sciences. 2025; 15(3):315-1. doi: 10.52711/2231-5659.2025.00046
Cite(Electronic):
Nikita Sawant, Bharati P. Caudhari, V. K. Redasani, Saniya Mulla. Documentation in Pharmaceutical Industry. Asian Journal of Research in Pharmaceutical Sciences. 2025; 15(3):315-1. doi: 10.52711/2231-5659.2025.00046 Available on: https://ajpsonline.com/AbstractView.aspx?PID=2025-15-3-13
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