Ministry of Pharmaceutical Industry National Agency of Pharmaceutical Products

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Guideline for the preparation and submission of registration, modification and renewal applications for pharmaceutical products for human use in Algeria

Guideline

Documents

ligne-directrice-pour-la-preparation-et-la-soumission-des-demandes-denregistrement-de-modification-et-de-renouvellement-des-produits-pharmaceutiques-a-usage-de-la-medecine-humaine-en-algerie.pdf (1.14 MB)

Record updated on 26 August 2026

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