Guidelines on Submission of Documentation for Registration of Herbal Medicinal Products for Human use |
Guidelines for Donation of Medical Products |
GUIDELINES FOR IDENTIFICATION AND LABELLING OF PHARMACEUTICAL PRODUCTS |
Guidelines for Introducting a Locally Manufactured New Human Medicinal Products to the Rwandan Market |
GUIDELINES FOR PRODUCT AND LOCATION MASTER DATA SHARING |
Guidelines for registration of medical products for unmet medical needs |
Guidelines for registration of similar Biotherapeutics Products |
Guidelines for the Cancellation_Suspension of a registered medical product |
Guidelines for variation of registered biological products |
Guidelines on Abridged Procedures for Pharmaceutical Products Assessment |
Guidelines on Reliance for Regulatory Decision-Making |
Guidelines on Submission of Documentation for Registration of Human Biological Products |
Guidelines on submission of documentation for registration_of human_medicinal products |
Guidelines on submission of documentation for Renewal of Registered Human and Veterinary Medicinal Products |
Rwanda FDA Guidelines for Good review practices |
Guidelines for Authorization for Emergency Use of Medicinal Products, Medical Devices and IVDS |
Guidelines on Submission of Documentation for Variations of Registered Human Medicinal Products |