Regulations
Laws, ordinances, decrees, orders, decisions, notes and guidelines governing pharmaceutical products and medical devices.
172 texts found
- Ligne directrice Guide on batch withdrawal and recall of non-compliant pharmaceutical products and medical devices Full text
- Ligne directrice Guide on the recall of batches and withdrawal of non-compliant pharmaceutical products and medical devices Full text
- Ligne directrice Algerian Guide to Good Pharmacovigilance Practices V2 Full text
- Ligne directrice Guideline on the risk-based classification of observations (deviations) arising from Good Manufacturing Practice (GMP) inspections of medicines for human use Full text
- Ligne directrice Guideline on recruitment and training Full text
- Ligne directrice Guideline on the requirements for bioequivalence and therapeutic equivalence studies Full text
- Ligne directrice Guideline on the prerequisites for renewing the registration decision Full text
- Ligne directrice Rules for drafting product information (SmPC, package leaflet and packaging) for medicines for human use Full text
- Ligne directrice Guideline for the preparation and submission of registration, modification and renewal applications for pharmaceutical products for human use in Algeria Full text
- Ligne directrice Guide to Good Distribution and Storage Practices for pharmaceutical products and medical devices for human use Full text
- Ligne directrice Guideline on communication Full text
- Ligne directrice Guideline on the refusal, temporary withdrawal and permanent withdrawal of the registration decision Full text
- Ligne directrice Guideline on defining the roles and responsibilities of the entities involved in the pharmaceutical product registration procedure within the ANPP Full text
- Note aux établissements 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 aux établissements 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