| DPT/DIV/-V4 |
Clinical Trial Causality Assessment Report |
Forms |
21/08/2025 |
Download
|
| 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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|
| DPT/DIV/--V4 |
CIOMS SERIOUS ADVERSE EVENTS (SAE) REPORTING FORM |
Forms |
21/08/2025 |
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|
| DD/PVCT/ GDL/ |
Guidance for Therapeutic or Vaccine Clinical Trial Application Evaluation During Public Health Emergency |
Guidelines |
21/08/2025 |
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|
| CBD/TRG/028 |
ADDENDUM TO THE REGULATION NO.: CBD/TRG/028 GOVERNING LICENSING TO MANUFACTURE, TO STORE, TO OPERATE AS WHOLESALE AND RETAIL SELLER OF PROCESSED FOODS AND RELATED PRODUCTS |
Regulations |
21/08/2025 |
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|
| FD/TRG/003-V4 |
REGULATIONS GOVERNING THE CONTROL OF PROCESSED FOOD PRODUCTS |
Regulations |
21/08/2025 |
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|
| DD/CHCR/GDL/001 |
GUIDELINES ON SUBMISSION OF DOCUMENTATION FOR REGISTRATION OF VECTOR CONTROL PRODUCTS AUGUST, 2025 |
Guidelines |
01/08/2025 |
Download
|
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