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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
  • Publications
    • All Publications
    • Policies, Legislation and Strategic Plan
      • Policies
      • Proclamations
      • Regulations
      • Strategic Plan
    • Directives and Guidelines
      • Medicine Directives
      • Medical Device Guidelines
      • Medicine Guidelines
      • Cosmetic Directive
      • Food Directives
      • Pharmacovigilance
      • Clinical Trials
    • Strategies
    • Manuals
    • Drugs lists and formularies
      • Drug Lists
      • Drug Formulary
    • Bulletins and Newsletter
      • Drug Bulletin
      • Food Bulletin
      • Pharmacovigilance Newsletter
      • EFDA Newsletter
    • 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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Pharmacovigilance newsletter Volume 1, Issue 1, 2022

By EFDADecember 21, 2022

Pharmacovigilance newsletter Volume 1, Issue 1, 2022

AEFI-Surviellance & response of AEFI guideline-3rd edition

By EFDAOctober 19, 2022

AEFI-Surviellance & response of AEFI guideline-3rd edition

ADE-ADR-ME-reporting form-EFDA

By EFDAOctober 19, 2022

ADE-ADR-ME-reporting form-EFDA

Addendum to AEFI Surveillance Guideline 2022

By EFDAOctober 19, 2022

Addendum to AEFI Surveillance Guideline 2022

AEFI standard reporting form Ethiopia

By EFDAOctober 19, 2022

AEFI standard reporting form Ethiopia

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

National-pharmacovigilance-Roadmap-2020

By EFDAApril 13, 2021

National-pharmacovigilance-Roadmap-2020

Covid-19 vaccine AEFI Reporting Form

By EFDAMarch 12, 2021

Covid-19 vaccine AEFI Reporting Form word document

Covid-19 vaccine AEFI Reporting Form

By EFDAMarch 12, 2021

Covid-19 vaccine AEFI Reporting Form

PV Newsletter V7 ISSUE 2 Feb 2020

By EFDAJuly 8, 2020

Pharmacovigilance newsletter No 2 2012

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