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Pharmaceutical facility design is a project carried by contributors from different scientific backgrounds’; like pharmacists, engineers, pharmaceutical machine suppliers and regulatory organizations such as Current Good Manufacturing Practices (cGMP), World Health Organization (WHO), International Standardization Organization (ISO), United States Pharmacopeia (USP), and many other ones. And by that nature, the project needs to be tackled form various approaches pharmaceutical approach, architectural engineering approach, and regulatory approach. This study will illuminate on the requirements in terms of regulations, design features, and equipment for a facility intended for manufacturing solid and liquid dosage forms of drugs under the regulations of Current Good Manufacturing Practices (cGMP).