2023.09.06 Guideline-for-WHO-Pre-qualified-Medicines-through-Collaborative-Registration-Procedure-
2023.09.06 Guideline-for-WHO-Pre-qualified-Medicines-through-Collaborative-Registration-Procedure-
2023.12.20 GUIDELINE FOR NON-ROUTINE REGISTRATION
2023.12.20 GUIDELINE FOR NON-ROUTINE REGISTRATION
2023.11.02 Guideline on Variation Application to Registered Medicines
2023.11.02 Guideline on Variation Application to Registered Medicines
2023.12.21 Guideline on Medical Products Special import permit
2023.12.21 Guideline on Medical Products Special import permit
2024.01.11 Guideline for control of advertising and promotion
2024.01.11 Guideline for control of advertising and promotion
2024.01.19 Guidance for Registration of Radiopharmaceuticals
2024.01.19 Guidance for Registration of Radiopharmaceuticals
2024.01.19 Guideline of Medicinal Gases Registration
2024.01.19 Guideline of Medicinal Gases Registration
2024.01.20 Guideline for Medicinal product information
2024.01.20 Guideline for Medicinal product information
2024.01.20 Guideline for preparation and publication of public assessment reports
2024.01.20 Guideline for preparation and publication of public assessment reports
2024.01.29 Guideline on Variation Applications to Registered Vaccines
2024.01.29 Guideline on Variation Applications to Registered Vaccines