Medical Device Registration and Approval in Algeria
General country-specific regulatory information is provided on this page for medical device registration and approval in Algeria.
Last updated on November 23rd, 2021.
Medical Device Regulations and Classification in Algeria
REGULATORY AUTHORITY: Regulation of medical devices in Algeria is conducted by the National Laboratory for the Control of Pharmaceutical Products (LNCPP), under the supervision of the Ministry of Health and Population.
CLASSIFICATION SYSTEM: The classification system is similar to the EU system (Classes I, IIa, IIb and III).
TIMEFRAME: The importation license takes 30 days to be issued. The registration timeline outlined by the LNCPP has not yet been implemented.
LICENSE VALIDITY: Licenses issued in Algeria expire after three years.
AUTHORIZED REPRESENTATIVE: A local representative is required to register medical devices in Algeria.
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