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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.
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.

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

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

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
Regulatory reform involves all stages of drug manufacturing, including facilitating investment, good distribution practices and export support.
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
Ministry of Pharmaceutical Industry © 2021. All rights reserved.