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የኢትዮጵያ ምግብና መድኃኒት ባለስልጣን
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Ethiopian Food and Drug Administration
EFDA
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  • Home
  • About Us
    • About EFDA
    • Our Vision, Mission and Objectives
    • Organizational Structure
    • Accreditations
    • Powers and Duties
  • News and Events
  • Services
    • Our Services
    • e-service
    • Traceability
      • FAQ’s
    • Electronic Regulatory Information System(eRIS)
    • How eRIS works
    • e-Reporting of ADR
    • Food Rapid Alert
    • Medical Device Safety
  • Publications
    • All Publications
    • Policies, Legislation and Strategic Plan
      • Policies
      • Proclamations
      • Regulations
      • Strategic Plan
    • Directives and Guidelines
      • Medicine Directives
      • Medical Device Guidelines
      • Medicine Guidelines
      • Medical Device Directives
      • Cosmetic Directive
      • Food Directives
      • Pharmacovigilance
      • Clinical Trials
      • Tobacco
    • Strategies
    • Manuals
    • Drugs lists and formularies
      • Drug Lists
      • Drug Formulary
    • Bulletins and Newsletter
      • Food Bulletin
      • Drug Bulletin
      • Pharmacovigilance Newsletter
      • EFDA Newsletter
      • Articles
    • Ethiopian Traceability System
  • Directorates
    • Director General
      • Food Sector Deputy Director General
      • Medicine Sector Deputy Director General
      • Medical Device Sector Deputy Director General
      • QMS Lead Executive Officer
      • Director General Office
      • Branch Coordination Lead Executive Officer
      • Intelligence & illegal Trade Prevention Lead Executive Officer
      • Chief Executive Officer
    • Medicine Sector Deputy Director General
      • Medicine Manufacturers Inspection and Enforcement Lead Executive Officer
      • Medicine Quality Control Lead Executive Officer
      • Medicine Registration & Market Authorization Lead Executive Officer
      • Pharmacovigilance & Clinical Trial Lead Executive Officer
    • Food Sector Deputy Director General
      • Food Registration and Licensing Lead Executive Officer
      • Food Safety and Quality Testing Lead Executive Officer
      • Food Inspection and Enforcement Lead Executives Officer
    • Medical Device Sector Deputy Director General
      • Medical Device Manufacturers Inspection and Enforcement Lead Executive Officer
      • Medical Device Quality Control Lead Executive Officer
      • Medical Device Registration & Market Authorization Lead Executive Officer
    • Chief Executive Officer
      • Basic Service Executive Officer
      • Competence & Human Resource Management Executive Officer
      • Information & Technology Executive Officer
      • Organizational Change Management Executive Officer
      • Procurement & Finance Executive Officer
      • Strategic Affair Executive Officer
      • Women & Inclusive Social Affair Executive Officer
    • Branch Office Head
      • Administration and Finance Team
      • Entry and Exit Products Inspection Lead Executive Officer
      • Food & Medicine Quality Control lead Executive Officer
      • Food Control Lead Executive Officer
      • Medicine & Medical Device Control Lead Executive Officer
  • COVID19
    • COVID19 FAQ’s
    • COVID19 publications
    • COVID-19 Quick Access
    • Privacy Policy
  • Public Information
    • Approved Medicine Product Information
      • Ethiopian Public Assessment Report
      • Summary of product characteristics
      • Patient information leaflets
    • Products and Institutions
    • Appointed Inspectors
    • Measure Taken
  • Announcement
    • Tender
    • Notices
    • Vacancy
  • Contact

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NCD PV guideline

By EFDAJune 2, 2023

NCD PV guideline

EFDA Vaccine Safety Risk and Crisis Communication Guideline

By EFDAJune 2, 2023

EFDA Vaccine Safety Risk and Crisis Communication Guideline

AEFI standard reporting form Ethiopia

By EFDAOctober 21, 2022

AEFI standard reporting form Ethiopia

Addendum to AEFI Surveillance Guideline 2022

By EFDAOctober 21, 2022

Addendum to AEFI Surveillance Guideline 2022

ADE-ADR-ME-reporting form-EFDA

By EFDAOctober 21, 2022

ADE-ADR-ME-reporting form-EFDA

Pharmacovigilance Directive No. 932/2022 932 የመድኃኒት ጎጂ ባህሪያት ክትትል ሥርዓት መመሪያ ቁጥር 932-2015

By EFDAOctober 17, 2022

932 የመድኃኒት ጎጂ ባህሪያት ክትትል ሥርዓት መመሪያ ቁጥር 932-2015

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