NameQuality Analysis Certificate Requirement for Exported Medical Products
DescriptionExported medical products must obtain a quality test certificate from the National Food and Drug Administration or an approved laboratory recognized by the Ministry of Health.
CommentsTo ensure product quality and consumer safety.
Validity From2025-08-25
ReferenceArticle 52 of Law 85/NA
Measure TypeTBT
AgencyMinistry of Health
Legal Document- Law on Drugs and Medical Products (Amendment) No.07/NA, Dated 10 March 2026
UN CodeP163
Procedures
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Forms
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Commodity/s
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