Regulations of Medical Devices are conducted by the Directorate of Pharmacy and by the National Laboratory for the Control of Pharmaceutical Products (LNCPP), which are both under the supervision of the Ministry of Health and Population. The registration process is conducted by submitting several documents to both bodies mentioned.

The classification system is similar to the EU system (Class I, IIa, IIb and III), but the CE mark or FDA clearance are not mandatory to the submission. As part of the registration process, the applicant must present a pricing structure for the product in question. Local representative must be assigned for the registration process.  Our country specific (*) regulatory services in Algeria include:

Medical Device specific regulation strategy reports in Algeria, Medical Device Registration with LNCPP and Directorate of Pharmacy, LNCPP Technical documents Preparation, license holder and local Authorized Representative in Algeria, QSD registration and Arazy Group unique line of GlobaR - Global Regulatory Hub™ products.

GlobaR Dossier™
GlobaR - One World Process™
GlobaR Submission Center ™
Universal Authorized Representative™

Please fill in the following form and submit your inquiry or discuss it with one of our online specialists. Let's get your products registered in Algeria!

(*) Algerian Regulatory Affairs services are part of the diverse professional consulting services provided by Arazy Group and can be found thorough this web site and inquired on through our form or online chat services.