Developing a Design Qualification Protocol as Standard Operating Procedure for a Pharmaceutical Plant Facility Meeting cGMP Requirement for Tablets and Capsules Manufacturing Department-Reference-Cited by-同舟云学术

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Developing a Design Qualification Protocol as Standard Operating Procedure for a Pharmaceutical Plant Facility Meeting cGMP Requirement for Tablets and Capsules Manufacturing Department

Published:2024 Issue: Volume: Page:229-326
ISSN:
Container-title:Modern Aspects of Pharmaceutical Quality Assurance
language:en
Short-container-title:

Author:

Bhusari Vidhya,Potdar Manohar,Nandalwar Pratiksha,Warbhe Prayas,Ghante Minal

Publisher

Springer Nature Singapore

Link

https://link.springer.com/content/pdf/10.1007/978-981-99-9271-3_8

Reference22 articles.

1. Heragu SS. Facilities design. 3rd ed. Boca Raton; 2008. p. 124–7.

2. Kovács G, Kot S. Facility layout redesign for efficiency improvement and cost reduction. J Appl Mat Comput Mech. 2017;16(1):63–74.

3. Potdar MA. Pharmaceutical facilities: design, layouts and validation. Hyderabad: PharmaMed Press; 2010. p. 40–94.

4. Chikwendu Okpala C, Okechukwu Chukwumuanya E, Chikwendu C. Plant layouts’ analysis and design modeling for sustainable municipal solid waste management view project industrial engineering plant layouts’ analysis and design. Int J Adv Eng Technol:11–25.

5. Greham C. Pharmaceutical production facilities design and application. 2nd ed. Taylor and Francis, British Pharmaceutic al Press; 1998. p. 370–98.

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1. Cybernetic Model Design for the Qualification of Pharmaceutical Facilities;Applied Sciences;2024-06-25

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