Role of Atomization in Pharmaceutical Industries

Authors

  • Nikita Bhojney
  • Shiv Hardenia
  • Dinesh Kumar Jain

DOI:

https://doi.org/10.62896/

Keywords:

Automation, Qualification, Quality assurance (QA), Research and development (R&D), Validation.

Abstract

Automating processes involves various control systems in industries with little to no human intervention to complete a variety of activities. The pharmaceutical industry has seen an increase in automation recently. Departments involved in manufacturing, packaging, labeling, and storage have all used automation. Manufacturing of specialized drugs is now possible thanks to automated equipment. Using the most recent technologies has had an impact on R&D as well. The SOP creation, auditing, qualifying, and equipment validation were the only conventional responsibilities of the QA department. The main focus of this study is relating to the use of automated technology in the pharmaceutical industry and how it affects the division in charge of pharmaceutical quality assurance. The Raman probe and other subjects are covered in this article. sDepartments involved in manufacturing, packaging, labeling, and storage have all used automation. The development of personalized pharmaceuticals has occurred as a result of the development of robotic devices. Therefore, these systems might be able to replace human inspectors. You can achieve greater accuracy and customization for a lower cost with this kind of technology.

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Published

2024-05-10

Issue

Section

Articles

How to Cite

Role of Atomization in Pharmaceutical Industries. (2024). International Journal of Pharmaceutical Drug Design, 1(05). https://doi.org/10.62896/

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