NAFDAC Pharmacovigilance and Post-Marketing Surveillance (PV/PMS) Directorate Guidelines for Post Marketing Surveillance in Nigeria
Ministry of Industry, Trade and Investment, National Agency for Food and Drug Administration and Control, Nigeria
The purpose of this guideline is to strengthen NAFDAC system for effective post marketing surveillance of medicines, and regulated products including medical devices to ensure that only quality and safe medicines and other regulated products are distributed throughout the country. The implementation of This guideline will enable NAFDAC generate scientific evidence on the quality and safety of medicines and medical devices for improved health outcome.
Process Flow
Department of Pharmacovigilance& Post Marketing Surveillance ⬤
Office of the Director General NAFDAC ⬤
Office of the Permanent Secretary, Ministry of Health ⬤
Office of the Minister of State for Health ⬤
Office of the minister for health ⬤
Federal Executive Council ⬤
Contacts
Fraden Bitrus
Deputy Director i/c
National Agency for Food and Drug Administration and Control (NAFDAC)
Moji Adeyeye
Director General
National Agency for Food and Drug Administration and Control (NAFDAC)
Mahmuda Mamman
Permanent Secretary
Ministry of Health
Adeleke O. Mamora
Honourable Minister of State
Ministry of Health
Osagie Ehanire
Honourable Minister
Ministry of Health
Muhammadu Buhari
President of the Federal Republic of Nigeria
NAFDAC Pharmacovigilance and Post-Marketing Surveillance (PV/PMS) Directorate Guidelines for Post Marketing Surveillance in Nigeria Current Version
January 2022
The purpose of this guideline is to strengthen NAFDAC system for effective post marketing surveillance of medicines, and regulated products including medical devices to ensure that only quality and safe medicines and other regulated products are distributed throughout the country. The implementation of This guideline will enable NAFDAC generate scientific evidence on the quality and safety of medicines and medical devices for improved health outcome.
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