Regulations

172 texts found

• Guideline Guide on batch withdrawal and recall of non-compliant pharmaceutical products and medical devices Full text
• Guideline Guide on the recall of batches and withdrawal of non-compliant pharmaceutical products and medical devices Full text
• Guideline Algerian Guide to Good Pharmacovigilance Practices V2 Full text
• Guideline Guideline on the risk-based classification of observations (deviations) arising from Good Manufacturing Practice (GMP) inspections of medicines for human use Full text
• Guideline Guideline on recruitment and training Full text
• Guideline Guideline on the requirements for bioequivalence and therapeutic equivalence studies Full text
• Guideline Guideline on the prerequisites for renewing the registration decision Full text
• Guideline Rules for drafting product information (SmPC, package leaflet and packaging) for medicines for human use Full text
• Guideline Guideline for the preparation and submission of registration, modification and renewal applications for pharmaceutical products for human use in Algeria Full text
• Guideline Guide to Good Distribution and Storage Practices for pharmaceutical products and medical devices for human use Full text
• Guideline Guideline on communication Full text
• Guideline Guideline on the refusal, temporary withdrawal and permanent withdrawal of the registration decision Full text
• Guideline Guideline on defining the roles and responsibilities of the entities involved in the pharmaceutical product registration procedure within the ANPP Full text
• Note to establishments 26-2026 Note No. 26-2026 on the publication of a guideline for the preparation and submission of registration, modification and renewal applications for pharmaceutical products Full text
• Note to establishments 27-2026 Note No. 27-2026 on the publication of a guideline defining the roles and responsibilities of the entities involved in the pharmaceutical product registration procedure Full text