Public Alert No. 041/2024 – Alert on the Recall of Nivea Roll-On Deodorant Due to Safety Concerns by European Union Rapid Alert System for Dangerous Non-Food Products (Rapex) Authorities
The National Agency for Food and Drug Administration and Control (NAFDAC) is alerting the public about the recall of Nivea BLACK &WHITE Invisible Roll-on deodorant, 50ml marked 48H Protection in African Climate with batch number: 93529610 by European Union (EU) Rapid Alert System for Dangerous Non-Food Products (RAPEX) in Brussels. The recalled Nivea product is said to […]
Public Alert No. 040/2024 – Alert on the Sale of Unregistered Simbrinza Eye Drop 10mg/ml + 2mg/ml (Brinzolamide+Brimonidine) in Nigeria
The National Agency for Food and Drugs Administration and Control (NAFDAC) wishes to inform the public about the sighting of unregistered Simbrinza Eye Drops with batch number VAF36C in Port Harcourt, Nigeria. The Marketing Authorization Holder (MAH) of the registered brand (Norvartis) reportedly sighted the unregistered brand of Simbrinza Eye Drops in Port Harcourt, Rivers […]
Public Alert No. 039/2024 – Alert on the Sale of Unregistered Foula Condom in Circulation in Nigeria
The National Agency for Food and Drug Administration and Control (NAFDAC) is alerting the public about the illegal sale and distribution of an unregistered brand of condoms in Nigeria: Foula Condoms. Officials from the Post-Marketing Surveillance (PMS) directorate discovered Foula condoms (packaged in threes) in Abakaliki, Ebonyi State, and Zango, Katsina State. This discovery was […]
Implementation of ICH Q1 and Q7 Guidelines
NAFDAC WORKSHOP ON ICH Q1 AND Q7 GUIDELINES AND ITS IMPLEMENTATION The National Agency for Food and Drug Administration and Control (NAFDAC), in partnership with Northeastern University, USA, and the International Council for Harmonization (ICH), successfully organized a workshop on ICH Q1 Stability Guidelines and ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients […]
Transition from the STED Format to the IMDRF-ToC Template for Submission of Technical Documents to Support the Registration of Medical Devices
The National Agency for Food and Drug Administration and Control (NAFDAC) was formally accepted by the International Medical Device Regulators Forum (IMDRF) as an Affiliate Member on the 22nd of March 2024. The IMDRF is a voluntary group of global medical device regulators worldwide who have come together to accelerate international medical device harmonization and […]
Report Of Risk-Based Post-Market Surveillance Of Selected Medical Products In Nigeria Carried Out In 2021, 2022 & 2023.
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International Council for Harmonization (ICH) Q1 Stability Guideline Workshop
Executive Summary for International Council for Harmonization (ICH) Q1 Stability Guideline Workshop Overview:The International Council for Harmonization (ICH) Q1 workshop was organized by the National Agency for Food and Drug Administration and Control (NAFDAC) supported by Northeastern University Boston USA and ICH, was held from 22nd-24th July 2024 at the Marriot Hotels Ikeja Lagos. The […]
International Council for Harmonization (ICH) Q7 (Good Manufacturing Practice Guideline for Active Pharmaceutical Ingredients) Training for Regulators and Industry
Executive Summary of the International Council for Harmonization (ICH) Q7 (Good Manufacturing Practice Guideline for Active Pharmaceutical Ingredients) Training for Regulators and Industry The recently concluded ICH Q7 training program, organized by NAFDAC and the Northeastern University Boston USA which was held from the 25th-26th July 2024, it successfully brought together regulators, industry professionals, academia […]
