الضوابط القانونية لعمل الوكالة الوطنية للمواد الصيدلانية في الجزائر

الملخص EN

The National Agency for Pharmaceutical Products is responsible for the registration, certification and control of pharmaceutical products and medical devices, and is responsible in particular for the registration of pharmaceutical products, the granting and renewal of the decision.

registration and, where applicable, suspension, withdrawal, allocation and transfer.

It after the opinion of the drug registration commission, in addition to quality control.

Provide expertise on pharmaceutical products and medical devices, and keep standard materials and reference products at the national level, in accordance with specific legal controls.

it is also responsible for performing audit and field inspection tasks carried out by inspectors affiliated with the Agency, and in particular for monitoring the application of good pharmaceutical practices and standards for medical devices in accordance with the applicable laws and regulations.