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The document outlines the registration requirements for pharmaceutical manufacturing sites with Jordan's Food and Drug Administration (JFDA). It lists 10 key requirements including: 1) Appointing a local Jordanian agent, 2) Preparing a site master file, 3) Providing a valid Good Manufacturing Practice (GMP) certificate, 4) Submitting a manufacturing license, 5) Providing a product list, 6) Detailing production lines in a table, 7) Submitting factory machinery lists, 8) Providing a facility layout, 9) Submitting GMP certificates from reference countries to avoid site inspection, and 10) Additional documents for contract manufacturers. It provides detailed instructions and notes for compiling registration files to meet all JFDA
The document outlines the registration requirements for pharmaceutical manufacturing sites with Jordan's Food and Drug Administration (JFDA). It lists 10 key requirements including: 1) Appoi…