General country-specific regulatory information is provided on this page for medical device registration and approval in Algeria.
We review our Regulatory Information frequently; please check back often for updates
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.
For detailed device-specific compliance information for each market, including Algeria, to expedite the preparation of your medical device or IVD registration application.
Did you know you can onboard your medical device or IVD compliance information to our system in less than 15 minutes?
And, in less than a minute, you can start your device-specific registration application and a complete county-specific registration process in this country or any of the other 140+ countries available for you through the Arazy Group Medtech registration platform.
