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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

Crossref DOI link: https://doi.org/10.1007/978-981-99-9271-3_8

Published Online: 2024-03-12

Published Print: 2024

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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