| 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 the Cancellation_Suspension of a registered medical product |
| Guidelines for variation of registered biological products |
| Guidelines_on_Abbreviated_Procedures_for_Pharmaceutical_Products_Registration |
| Guidelines on Reliance for Regulatory Decision-Making |
| Guidelines for registration of Human Biological 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 for Variation to Registered Human Pharmaceutical Products |
| Guidelines for Registration of Pharmaceutical Products |
| Guidelines for Registration of Biosimilar Products |
Toll Free: 9707
info@rwandafda.gov.rw
Nyarutarama Plaza, KG 9 Avenue
