Abstract
This article provides an overview of an IT tool that addresses the process documentation and recipe preparation and approval process in a multi-product, multi-purpose, bulk pharmaceutical manufacturing facility. The article concludes by forwarding a proposal outlining a road map for development of an equivalent Off-The-Shelf ISA Standard S88 compliant application.
Original language | English |
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Pages (from-to) | 28-44 |
Number of pages | 16 |
Journal | Pharmaceutical Engineering |
Volume | 21 |
Issue number | 3 |
Publication status | Published - May 2001 |