| LSD/VBT/GDL/001 |
Guidelines-Governing-LR_Final-draft (1).docx |
Guidelines |
01/12/2026 |
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| ODG/QMS/FMT/023-1 |
Providing comment on document under development process |
Forms |
24/02/2026 |
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| DD/VMDR/FMT/027-1 |
Cover Letter for Application of Notification of Veterinary Medical Devices and In Vitro Diagnostic Devices |
Forms |
12/02/2026 |
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| DD/VMDR/GDL/008 |
Guideline for Notification of Veterinary Medical Devices and In Vitro Diagnostic Devices |
Guidelines |
12/02/2026 |
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| DD/VMDR/FOM/006 |
Notification Application Form of Veterinary Medical devices and or In Vitro Diagnostics Devices (IVDD) |
Forms |
12/02/2026 |
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| DD/PIL/5565/FDA/2025 |
Circular on Public consultation and call for comments on regulatory documents |
Guidelines |
31/12/2025 |
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| DD/PIL/TRG/005-Rev_5 |
REGULATIONS GOVERNING THE LICENSING OF PUBLIC AND PRIVATE MANUFACTURERS, DISTRIBUTORS, WHOLESALERS AND RETAILERS OF MEDICAL PRODUCTS |
Regulations |
18/12/2025 |
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| DD/PIL/GDL/005-Rev_5 |
GUIDELINES FOR LICENSING OF PUBLIC AND PRIVATE MANUFACTURERS, DISTRIBUTORS, WHOLESALERS AND RETAILERS OF HUMAN MEDICINES |
Guidelines |
18/12/2025 |
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| WWW/XXX/YYY/ZZZ-HM-1 |
GUIDELINES FOR CHANGE TO REGISTERED OR NOTIFIED MEDICAL DEVICES |
Guidelines |
17/12/2025 |
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| DAR/GDL/075-Version-3 |
GUIDELINES FOR REGISTRATION OF IN VITRO DIAGNOSTICS DEVICES |
Guidelines |
17/12/2025 |
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| DHT/GDL/024-Version-2 |
GUIDELINES FOR REGISTRATION OF MEDICAL DEVICES |
Guidelines |
17/12/2025 |
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| WWW/XXX/YYY/ZZZ-HM-2 |
GUIDELINES FOR REVIEW AND APPROVAL OF SOFTWARE AS MEDICAL DEVICES (SaMD) |
Guidelines |
17/12/2025 |
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| DD/PVCT/GDL/008-V4 |
Guidelines for Review and Approval of Clinical Trials |
Guidelines |
21/08/2025 |
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| DD/PVCT/GDL/005-V4 |
Guidelines for Clinical Trials Applications in Rwanda |
Guidelines |
21/08/2025 |
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| DD/PVCT/FOM/007 |
CLINICAL TRIAL APPLICATION FORM |
Forms |
21/08/2025 |
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