{"id":22062,"date":"2025-12-25T01:35:11","date_gmt":"2025-12-25T00:35:11","guid":{"rendered":"https:\/\/anpp.dz\/missions\/"},"modified":"2025-12-25T01:35:11","modified_gmt":"2025-12-25T00:35:11","slug":"missions","status":"publish","type":"page","link":"https:\/\/anpp.dz\/en\/missions\/","title":{"rendered":"Missions"},"content":{"rendered":"

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Our Missions<\/h1>\n\t\t<\/div>\n\t\t[vc_row_inner][vc_column_inner width=”1\/3″][mvc_infobox link=”link_box” title_color=”#000000″ info_title=”Enregistrement des Produits Pharmaceutiques” image_size=”150″ btn_url=”url:%23″ image_id=”21242″ caption_url=””][\/mvc_infobox][\/vc_column_inner][vc_column_inner width=”1\/3″][mvc_infobox link=”link_box” title_color=”#000000″ info_title=”Homologation des Dispositifs M\u00e9dicaux” image_id=”21244″ image_size=”150″ btn_url=”url:%23″ caption_url=””][\/mvc_infobox][\/vc_column_inner][vc_column_inner width=”1\/3″][mvc_infobox link=”link_box” title_color=”#000000″ info_title=”Contr\u00f4le de la Qualit\u00e9 et de l’Expertise” image_id=”21246″ image_size=”150″ btn_url=”url:%23″ caption_url=””][\/mvc_infobox][\/vc_column_inner][\/vc_row_inner][vc_row_inner][vc_column_inner][\/vc_column_inner][\/vc_row_inner][\/vc_column][\/vc_row][vc_row][vc_column][vc_column_text css=””]<\/p>\n

Missions Principales<\/h2>\n\n

Registration of pharmaceutical products<\/strong> and granting of the registration decision, its renewal, suspension, withdrawal, assignment, and transfer, following the opinion of the Pharmaceutical Products Registration Committee.<\/p>\n\n

Approval of medical devices<\/strong> and granting of the approval decision, its renewal, suspension, withdrawal, assignment, and transfer, following the opinion of the Medical Devices Approval Committee.<\/p>\n\n

Quality control and expertise<\/strong> of pharmaceutical products and medical devices, and maintenance of reference substances and standard products at the national level.<\/p>\n\n

Conducting audit and inspection missions on-site<\/strong>, carried out by agency inspectors, particularly to verify the implementation of good pharmaceutical practices and medical device standards, in accordance with the applicable legislation and regulations.<\/p>\n\n

Contributing to the development<\/strong> strategies of the pharmaceutical sector.<\/p>\n\n

Referring matters<\/strong> to the competent authorities in order to take the necessary measures to protect public health when a pharmaceutical product or medical device presents or is suspected of presenting a risk to human health.<\/p>\n\n

Issuing opinions<\/strong> on Temporary Authorizations for Use (ATU)<\/strong> for unregistered medicines.<\/p>\n\n

Contributing to the definition of Good Practices<\/strong> for the manufacturing, storage, distribution, and dispensing of pharmaceutical products.<\/p>\n\n

Conducting scientific evaluations<\/strong> of the benefits, risks, and therapeutic value of pharmaceutical products and medical devices, as well as their health-economic assessment.<\/p>\n\n

Contributing<\/strong> to the establishment and updating of nomenclatures for pharmaceutical products and medical devices.<\/p>\n\n

Contributing to the development<\/strong> of the list of essential pharmaceutical products and medical devices.<\/p>\n\n

Contributing to the preparation<\/strong> of the national medicines formulary and the pharmacopoeia.<\/p>\n\n

Issuing price certificates for medicines at the time of registration, once prices are determined by the Intersectoral Economic Committee for Medicines.<\/p>\n\n

Participating in the preparation<\/strong> of the list of medicines reimbursable by social security organizations.<\/p>\n\n

Issuing prior authorizations<\/strong> for the promotion and advertising of registered pharmaceutical products directed to health professionals.<\/p>\n\n

Providing opinions on requests<\/strong> for conducting clinical trials and bioequivalence studies.<\/p>\n\n

Providing opinions<\/strong> on standards, good practice rules, procedures, and methods applicable to clinical studies involving pharmaceutical products and medical devices.<\/p>\n\n

Undertaking <\/strong>studies, research, training, and information activities within its fields of competence, contributing to the promotion of scientific research related to pharmaceutical products and medical devices, and establishing the relevant databases.<\/p>\n\n

Organizing <\/strong>seminars, conferences, study days, and other events related to its missions.<\/p>\n\n

Participating in the drafting of legislative and regulatory texts governing pharmaceutical products and medical devices.<\/p>\n\n

Implementing <\/strong>international cooperation actions, in accordance with applicable legislation and regulations.<\/p>\n\n

Preparing an annual <\/strong>activity report submitted to the Minister in charge of the Pharmaceutical Industry.<\/p>\n

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