Health
Nigeria joins global ICH elite as NAFDAC achieves full international regulatory Status
Nigeria joins global ICH elite as NAFDAC achieves full international regulatory Status
Nigeria has recorded a major milestone in global health regulation as the National Agency for Food and Drug Administration and Control (NAFDAC) has secured full membership of the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH). The achievement positions Nigeria among the world’s most advanced national regulatory authorities and marks a transformative step for the country’s pharmaceutical sector.
The announcement was made during the ICH Assembly held in Singapore, where Nigeria was confirmed as the 24th out of only 25 national regulatory authorities (NRAs) globally recognised for their commitment to harmonised international pharmaceutical standards.
NAFDAC Director General, Prof. Moji Adeyeye, described the development as a “historic breakthrough for Nigeria and the African continent,” noting that full membership would significantly boost the availability of high-quality, safe, and effective medicines for Nigerians.
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She said:
“Full ICH membership means Nigerians will have better access to high-quality medicines. It confirms that our regulatory scientists can stand shoulder-to-shoulder with the best in the world.”
Nigeria’s journey to full ICH status began in 2022 after the agency secured Observer status and later participated in the 2023 ICH meeting in Vancouver, Canada, where NAFDAC made a formal presentation as part of the evaluation process.
Over the last two years, NAFDAC underwent extensive capacity-building, including training on multiple ICH guidelines, membership in expert working groups, and the hosting of a major international workshop in Lagos in April 2025 on the ICH M13A Bioequivalence Guideline.
Adeyeye credited the agency’s success to a “methodical and structured approach,” supported by Northeastern University, Boston, and the Bill & Melinda Gates Foundation.
Nigeria’s Ambassador to Singapore, H.E. Omayuli Francisca Kemi, praised NAFDAC for demonstrating “leadership, resilience, and expertise” in earning a place on the global regulatory stage.
Full ICH membership grants NAFDAC authority to contribute directly to the formulation of international pharmaceutical standards, while enhancing Nigeria’s capacity to regulate medicines, accelerate access to innovative therapies, and improve confidence in local pharmaceutical manufacturing.
Adeyeye also acknowledged the Federal Government for extending her tenure, saying the continuity was crucial to achieving this milestone.
“We will continue to safeguard the health of the nation—now with the full strength of the ICH global community behind us,” she declared.
NAFDAC expressed appreciation to President Bola Ahmed Tinubu, the Minister of Health and Social Welfare, and its international partners for their support. The agency reaffirmed its commitment to full implementation of ICH standards, strengthening Nigeria’s regulatory system, and advancing pharmaceutical innovation and production.
Nigeria Joins Global ICH Elite as NAFDAC Achieves Full International Regulatory Status
Health
China Unveils Blink-Powered Device to Aid Paralysed Patients’ Mobility
China Unveils Blink-Powered Device to Aid Paralysed Patients’ Mobility
Chinese researchers have unveiled a groundbreaking blink-powered eye-tracking device designed to help paralysed patients regain control over wheelchairs and assistive devices. The innovation captures energy generated by blinking to operate devices, offering new independence for individuals with ALS, spinal injuries, and severe mobility impairments.
The device, named ET‑TENG, uses a triboelectric nanogenerator (TENG) to convert eyelid movements into electrical signals, allowing users to navigate wheelchairs or communicate with technology without external batteries. Unlike traditional camera-based eye-tracking systems, ET‑TENG functions even in total darkness, making it more reliable for daily use.
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Developed through collaboration between Qingdao University and the Hong Kong University of Science and Technology, ET‑TENG demonstrated 99% accuracy in detecting eye movements as small as 2 degrees, ensuring precise control for patients. Experts say this technology could significantly improve quality of life and autonomy for people living with paralysis.
This innovation is part of a growing wave of assistive technologies and brain-computer interfaces (BCI) in China and globally, aimed at translating neuroscience breakthroughs into practical tools for patients with severe disabilities. Researchers hope ET‑TENG and similar devices will soon allow users to communicate, move independently, and interact with the world in ways that were previously impossible.
China Unveils Blink-Powered Device to Aid Paralysed Patients’ Mobility
Health
Father Blames Lagos Health Centre After Twin Infants Die Following Immunisation
Father Blames Lagos Health Centre After Twin Infants Die Following Immunisation
A grieving father has accused a Lagos health centre of negligence following the death of his nine-month-old twin boys, who reportedly died hours after receiving routine vaccination at a government-owned facility in the state.
The father, Samuel Alozie, said he took the twins to the Ajangbadi Primary Health Centre in Ojo Local Government Area for their scheduled immunisation. According to him, the babies were healthy and active before the visit but developed severe reactions shortly after the injections.
He alleged that the twins became unusually weak, stopped feeding properly and failed to respond to treatment given at home based on advice from health workers. Tragically, both children reportedly died within 24 hours of receiving the vaccines.
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The incident, which has sparked widespread outrage on social media, has raised fresh concerns about vaccine safety, medical negligence, and standards of care at public health facilities in Lagos State. In emotional online videos, the father questioned the drugs administered to his children and called for a transparent investigation, insisting that the deaths were preventable.
Reacting to public pressure, the Lagos State Government ordered a post-mortem examination to determine the exact cause of death. Officials said the autopsy would establish whether the fatalities were linked to the vaccination, medical error, or other underlying health conditions.
Health authorities have urged the public to remain calm while investigations continue, noting that routine childhood immunisation remains safe and critical in preventing deadly diseases. However, rights groups and concerned parents are demanding accountability, insisting that any form of medical malpractice uncovered must be prosecuted.
The tragic deaths have reignited national debate on healthcare delivery in Nigeria, particularly in primary health centres, with many Nigerians calling for better training, monitoring and equipment to prevent similar incidents in the future.
Father Blames Lagos Health Centre After Twin Infants Die Following Immunisation
Health
NAFDAC Reassures Nigerians as Nestlé Recalls SMA Infant Formula in 50 Countries
NAFDAC Reassures Nigerians as Nestlé Recalls SMA Infant Formula in 50 Countries
The National Agency for Food and Drug Administration and Control (NAFDAC) has reassured Nigerians that Nestlé infant formula products approved for sale in Nigeria are safe, following public concern over a voluntary global recall of SMA Infant Formula in more than 50 countries.
In a statement issued by the NAFDAC Director-General, Prof. Mojisola Adeyeye, the agency clarified that the recall by Nestlé UK was limited to specific batches overseas and does not affect products available in the Nigerian market.
According to NAFDAC, the recall was prompted by the potential presence of cereulide, a toxin that can cause nausea and vomiting, in some UK-manufactured batches. Cereulide is described as a heat-resistant toxin produced by certain strains of the bacterium Bacillus cereus.
“The Agency wishes to reassure the public, healthcare professionals and relevant stakeholders, particularly parents, guardians and caregivers, that all Nestlé infant formulae currently approved for marketing in Nigeria are safe for consumption and are not part of the recall,” the statement said.
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NAFDAC explained that the SMA infant formula sold in Nigeria is manufactured at the Nestlé Tuas Factory in Singapore and is fully registered and approved by the agency. It further confirmed that both the SMA and NAN ranges produced for the Nigerian market are not among the affected batches involved in the voluntary recall abroad.
The agency noted that the public advisory was issued purely as a precautionary public health measure, in line with NAFDAC’s mandate to keep Nigerians informed of global food safety developments, even where the risk of local exposure is low.
However, NAFDAC warned that potential risks could still arise through unauthorised importation, online purchases, or personal carriage of recalled products during international travel.
The agency assured Nigerians that it remains vigilant and committed to ensuring the safety of food and pharmaceutical products in Nigeria, while continuing to monitor global developments related to infant nutrition and food safety.
NAFDAC Reassures Nigerians as Nestlé Recalls SMA Infant Formula in 50 Countries
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