Medical Device Registration in Algeria | MOH Approval Support – Operon Strategist

 Operon Strategist provides expert consulting for medical device registration in Algeria, ensuring smooth regulatory approval from the Ministry of Health (MOH). Our team supports manufacturers with accurate device classification, preparation of technical documentation, dossier submission, and compliance with import regulations. We help companies navigate Algeria’s complex medical device laws, including labeling requirements in Arabic and French, and import restrictions for unregistered devices. Beyond regulatory consulting, Operon Strategist offers turnkey project management services, including cleanroom design, facility setup, and quality system implementation. With our end-to-end support, Algerian and international manufacturers can fast-track product approvals, achieve regulatory compliance, and successfully launch their medical devices in the Algerian market.

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