| 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 |
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|
| DD/CHCR/GDL/003 |
GUIDELINES ON SUBMISSION OF DOCUMENTATION FOR REGISTRATION OF PUBLIC HEALTH ANTISEPTIC AND DISINFECTANT PRODUCTS |
Guidelines |
01/08/2025 |
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|
| DD/CHCR/GDL/006 |
GUIDELINES ON VARIATION APPLICATION OF REGISTERED COSMETICS, VECTOR CONTROL AND PUBLIC HEALTH LABORATORY CHEMICAL PRODUCTS |
Guidelines |
01/08/2025 |
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| DD/CHCR/GDL/002 |
GUIDELINES ON SUBMISSION OF DOCUMENTATION FOR REGISTRATION OF COSMETIC PRODUCTS |
Guidelines |
01/08/2025 |
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|
| DPT/DIV/DOC.TYPE/XXX |
SERIOUS ADVERSE EVENTS (SAE) REPORTING FORM |
Forms |
01/08/2025 |
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|
| DD/PVCT/TRG/001-V4 |
REGULATIONS GOVERNING THE CONDUCT AND INSPECTION OF CLINICAL TRIALS IN RWANDA |
Guidelines |
01/08/2025 |
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|
| 002-V4 |
Draft-Veterinary-pesticide-Good-Manufacturing-Practice-inspection-guidelines-Annex.docx |
Guidelines |
01/08/2025 |
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|
| WWW/XXX/YYY/ZZZ |
Guidelines for Registration of Innovative Human Medical Products |
Guidelines |
05/06/2025 |
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|
| DD/VMDR/GDL/001-V2 |
GUIDELINES FOR REGISTRATION OF VETERINARY PHARMACEUTICAL PRODUCTS |
Guidelines |
06/02/2025 |
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|
| DD/VMDR/GDL/004-V2 |
GUIDELINES FOR REGISTRATION OF VETERINARY BIOLOGICAL PRODUCTS |
Guidelines |
06/02/2025 |
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|
| FD/TRG/007 |
Regulations-for-Processed-food-products |
Regulations |
06/02/2025 |
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|