Amendments to the Standards of Medical Device Good Manufacturing Practices; (11 page(s), in English)
FDA Circular: Guidelines on the Maintenance of Importation and/or Distribution Records, and the Reporting of Product Complaints, Adverse Events, and Field Safety Corrective Actions for Medical Devices; (15 page(s), in English)
Medicines Amendment Bill 2025 ; (14 page(s), in English)
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