• 16/02/2026: Le ministre de l’Industrie pharmaceutique, Dr. Wassim Kuidri, préside au siège du ministère une réunion de coordination des membres du groupe de travail national multisectoriel et multidisciplinaire chargé de suivre le projet de création d’un centre intégré de recherche en virologie et d’une usine de production de vaccins.

Industrial Policy

Axis 1 :
Ensuring the continuous availability of pharmaceutical products, with a particular focus on essential medicines.

Through the creation of a monitoring and surveillance device for the availability of pharmaceutical products, Continuous monitoring of import and domestic production programs, the updating of the essential medicines list, and the evaluation of import volumes according to market demand and current stock levels.

Axis 2 :
Implementation of tools and a regulatory framework to ensure quality, efficiency, and safety


The National Agency for Pharmaceutical Products ANPP is strengthened in human and material resources, the drug registration and medical device approval commissions, sits on the intersectoral economic committee for medicines as well as the committee of clinical experts.

Through the implementation of a new pricing procedure, the prioritization of the registration of generic medicines and similar biotherapeutic products, and the improved management of raw material import programmes.

Axis 4 :
Guaranteeing equitable and affordable access to pharmaceutical products for all citizens

By expediting the approval process for pharmaceutical establishments, encouraging subcontracting, and promoting exports through the redirection of several investment projects towards local manufacturing for export purposes.

The public group Saidal is benefiting from a development plan designed to establish it as a public hub ensuring national health sovereignty.

Plateforms

Plateform " تبادل-إنتاج "

Online submission of digitized application files for the licensing of pharmaceutical establishments and the manufacturing of pharmaceutical products and medical devices.
tabadol@miph.gov.dz

Plateform "رؤية"

Improves visibility on the status of medicine stocks throughout the supply chain through:
1-Monthly stock declarations;
2-Reporting of provisional programs;
3-Monthly reporting on implementation progress. ........More information

Plateform "تبادل "

Online submission of digitized application files for the licensing of pharmaceutical establishments, import, exploitation, and wholesale distribution of pharmaceutical products and medical devices, Or by email for approval renewals: tabadol@miph.gov.dz

Collection of legal texts

Regulatory reform involves all stages of drug manufacturing, including facilitating investment, good distribution practices and export support.

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The application for a license for a pharmaceutical establishment The application for a license for a pharmaceutical establishment must be accompanied by a file containing the following documents: >> read more.
As part of the promotion of clinical studies, research, and development, the Ministry of the Pharmaceutical Industry is planning favorable measures to support clinical research activities and innovation in the pharmaceutical industry.​
As part of the action plan of the Ministry of Pharmaceutical Industry, the promotion of exports is s a major focus for the development of the sector and its transformation from a budget-consuming sector to a wealth-creating sector.
List of Pharmaceutical Establishments Approved by the Ministry of Pharmaceutical Industry
A systematic, continuous, ethical, and legal process for collecting, analysing, processing, and disseminating information.
Serialization is the process of assigning unique identifiers to individual products and/or individual product packages in order to be able to readily identify and track the products and/or packages. Serialization bestows a unique, protected identity to each serialized item.

Pharmaceutical establishments are requested to submit their observations regarding the nomenclature of their pharmaceutical products within one (1) month from the date of publication of the latest version of the National Nomenclature of Pharmaceutical Products for Human Use

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