Jordan has released draft instructions establishing a comprehensive framework for the licensing, registration, import, distribution, and post-market oversight of pharmaceutical and cosmetic products. The framework outlines regulatory procedures, documentation requirements, approval pathways, and compliance obligations for manufacturers, importers, distributors, and marketing authorization holders. It also strengthens requirements related to GMP compliance, product traceability, labeling, import/export controls, lifecycle management, and post-marketing surveillance. In addition, the draft enhances inspection and enforcement measures, including product recalls, suspension, and import restrictions for non-compliance. Overall, the mandate aims to improve regulatory oversight, product quality, supply chain transparency, and patient safety in Jordan.
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