Regulations

141 texts found

• Note aux établissements 40-2025 Note No. 40-2025 on the filing of approval files for marketed non-approved medical devices (22-09-2025) Full text
• Note aux établissements 41-2025 Note No. 41-2025 on the launch of the E-TASJIL V2 platform Full text
• Note aux établissements 45-2025 Note No. 45-2025 on the guidelines for bioequivalence studies 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
• Note aux établissements 28-2026 Note No. 28-2026 on the procedures for filing medical device approval files in digital format Full text
• Note aux établissements 29-2026 Note No. 29-2026 on the implementation of the Algerian Guide to Good Pharmacovigilance Practices Full text
• Note aux établissements 30-2026 Note No. 30-2026 on the profile of the QPPV within the framework of implementing the Algerian Guide to Good Pharmacovigilance Practices Full text
• Note aux établissements 33-2026 Note No. 33-2026 on the publication of a guideline for laboratory testing of pharmaceutical products Full text
• Note aux établissements 34-2026 Note No. 34-2026 on the admissibility of pharmaceutical product registration files Full text
• Note aux établissements 36-2026 Note No. 36-2026 on regulatory reliance and recognition in the context of registering pharmaceutical products and modifying registration decisions Full text
• Note aux établissements 37-2026 Note No. 37-2026 on regulatory reliance practices in pharmacovigilance Full text
• Note aux établissements 38-2026 Note No. 38-2026 on the modification of pharmaceutical product registration decisions Full text
• Note aux établissements 39-2026 Note No. 39-2026 on lifting reservations issued on medical device approval files Full text
• Note aux établissements 41-2026 Note No. 41-2026 on product classification requests Full text