| 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 |
Toll Free: 9707
info@rwandafda.gov.rw
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