| 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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|
| DPT/DIV/-V4 |
Clinical Trial Causality Assessment Report |
Forms |
21/08/2025 |
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| DD/PVCT/FMT/037 |
CLINICAL TRIAL PROTOCOL |
Forms |
21/08/2025 |
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| DD/PVCT/FOM/034 |
DECLARATION BY PI OR CO-PI |
Forms |
21/08/2025 |
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|
| DD/PVCT/ GDL |
Guidance for Therapeutic or Vaccine Clinical Trial Application Evaluation During Public Health Emergency 2 |
Guidelines |
21/08/2025 |
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|
| DD/PVCT/GDL/013 |
Guidelines for Monitoring and Reporting Clinical Trial Safety Data in Rwanda |
Guidelines |
21/08/2025 |
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| DD/PVCT/GDL/005 |
Guidelines for Clinical Trials Applications in Rwanda |
Guidelines |
21/08/2025 |
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|
| DD/PVCT/GDL/008 |
Guidelines for Review and Approval of Clinical Trials |
Guidelines |
21/08/2025 |
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|
| DD/PVCT/FMT/038 |
INVESTIGATIONAL PRODUCT QUALITY OVERALL SUMMARY |
Forms |
21/08/2025 |
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|
| DD/PVCT/FOM/033 |
JOINT DECLARATION FOR SUFFICIENT FUNDS |
Forms |
21/08/2025 |
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|
| DD/PVCT/TRG/001 |
Regulations Governing the Conduct and Inspection of Clinical Trials in Rwanda |
Regulations |
21/08/2025 |
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|
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