• Twitter
  • Facebook
  • Youtube
  • LinkedIn
  • Mail
Rwanda FDA
  • Welcome
  • About FDA
    • Overview
    • Senior management
    • Board of Directors
    • Departments
      • Office Of Chief Finance
      • Food and Drugs Inspection and Safety Monitoring
      • Food and Drugs Assessment and Registration (FDAR)
    • Organization Structure
    • Laws
    • Quality Management System
    • Quality Control Laboratory
    • Reports
    • Stakeholders
  • Medicine
    • Registration
      • Human Medicine
        • Regulations
        • Guidelines
        • Guidance
        • Forms and Format
        • Registered Products
        • Unregistered Products
        • Summary of Products Characteristics (SmPC)
        • Patient Information Leaflet (PIL)Summary of Products Characteristics
        • Circular
      • Veterinary medicine
        • Regulations
        • Guidelines
        • Forms and Format
        • Registered Products
        • Unregistered Products
        • Summary of Products Characteristics
        • Circulars
    • Inspection
      • Regulations
      • Guidelines
      • Forms
      • Requirements
      • Licensed Premises
      • Revoked Premise License
      • Suspended Premise License
      • List of complied GMP Manufacturers
      • Circular on recalled products
    • Import and Export
      • Regulations
      • Guidelines
      • Requirements
    • Post market Surveillance
      • Regulations
      • Guidelines
      • Post marketing surveillance committee
      • Recalled products
      • Quarantined products
      • Forms
    • Promotion and advertisement control for medical products
      • Regulations
      • Guidelines
      • Forms
      • Application requirements
  • Food
    • Registration
      • Food
        • Laws and Regulations
        • Guidelines
        • Forms and Formats
        • Registered Products
      • Feed
        • Regulations
        • Forms and format
    • Inspection
      • Regulations
      • Guidelines
      • Requirements
      • Forms
      • Registered and licensed premises
    • Import and export
      • Regulations
      • Guidelines
      • Guidances
      • Requirements
    • Food safety surveillance
      • Food safety information
      • Guidelines
      • Recalled food products
    • Promotion and advirtesment control for food products
      • Regulations
      • Guidelines
      • Application Requirements
      • Application forms
  • Medical Cosmetics &Households Chemicals
    • Registration
      • Medicated Cosmetics Registration
        • Regulations
        • Guidelines
        • Requirements
        • Forms
      • Antiseptics and disinfectants
        • Regulations
        • Guidelines
        • Requirements
        • Forms
      • Household Pesticide Registration
        • Regulations
        • Guidelines
        • Requirements
        • Forms
      • Cleaning Chemicals Registration
        • Regulations
        • Guidelines
        • Requirements
        • Forms
      • Laboratory Chemicals Registration
        • Regulations
      • Registered products
      • Unregistered Products
    • Inspections
      • Regulations
      • Guidelines
      • Forms
      • Registered and licensed premises
    • Import and Export
      • Regulations
      • Guidelines
      • Requirements
  • Medical Devices
    • Registration
      • Human Medical Devices and In-Vitro Diagnostics
        • Regulations
        • Guidelines
        • Circulars
        • Forms
      • Veterinary Medical Devices and In-Vitro Diagnostics
        • Regulations
        • Guidelines
        • Forms
        • Circulars
    • Inspection
      • Regulations
        • Forms
      • Guidelines
      • Requirements
      • Premise registration and licensing
    • Import and Export
      • Regulations
      • Guidelines
      • Requirements
  • Clinical Trials and Vigilance
    • Clinical Trial Oversight
      • Regulations
      • Guidelines
      • Clinical Trial Forms
      • Register of clinical trials
    • Vigilance
      • Regulations
      • Guidelines
      • Medicine safety bulletin
      • Reporting forms
      • Safety Information
      • Advisory committee
  • Tobacco
    • Registration
      • Import and Export
      • Laws and Regulations
      • Forms and formats
    • Import and Export
      • Guidelines
  • Contact
  • Search
  • Menu Menu

Clinical Trial Oversight Register

Names
Clinical trial Register of Authorized Clinical trials-September version 2022

The mandate of the Authority is to protect public health through regulation of human and veterinary medicines, vaccines and other biological products, processed foods, poisons, medicated cosmetics, medical devices, household chemical substances, tobacco and tobacco products.

CONTACT US

Toll Free: 9707

info@rwandafda.gov.rw

Nyarutarama Plaza, KG 9 Avenue

 

Social Media

   

Useful links

  • Ministry of Health
  • Rwanda Biomedical Centre
  • Rwanda Government
  • World Health Organization
  • Staff mail

 

Our Accounts

  1. BNR:1000047658 entitled “Rwanda FDA” in FRW
  2. BNR:1000047666 entitled “Rwanda FDA” in USD, Swift Code:BNRWRWRW
  3. BK:100025143684 entitled “Rwanda FDA” in FRW
  4. BK:100025143765 entitled “Rwanda FDA” in USD, Swift Code: BKIGRWRW
© 2022 Rwanda Food and Drug Authority
  • Twitter
  • Facebook
  • Youtube
  • LinkedIn
  • Mail
Scroll to top