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Mojisola Christianah Adeyeye
Mojisola Christianah Adeyeye is a Nigerian pharmacist, pharmaceutical-science academic and public regulator. Reporting from July 2026 identified her as Director-General of Nigeria's National Agency for Food and Drug Administration and Control, which she was first appointed to lead in 2017 after an academic career in pharmaceutics and drug-product evaluation.
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Nigeria · Pharmacist, Pharmaceutical-science academic, Public regulator · 1 affiliation
Adeyeye's initial five-year appointment as NAFDAC Director-General took effect on 3 November 2017. Reporting later described a second five-year tenure as effective from 1 December 2022, while a separate February 2024 report said President Bola Tinubu had reappointed her amid changes in health-sector leadership. July 2026 reporting continued to identify her as Director-General, although the available evidence does not establish the precise legal structure or end date of her current tenure.
A UNIDO-hosted biography states that Adeyeye earned a bachelor's degree from the University of Nigeria, Nsukka, followed by master's and doctoral degrees from the University of Georgia in Athens. It also identifies her as Professor Emeritus of Pharmaceutics and Drug Product Evaluation at Roosevelt University, founding chair of its Biopharmaceutical Sciences unit, and a former Professor of Pharmaceutics and Manufacturing at Duquesne University, where she worked for 21 years.
Several institutional milestones occurred during Adeyeye's leadership of NAFDAC. WHO announced in March 2022 that Nigeria's regulator had attained maturity level 3 for medicines and imported-vaccine regulation, and WHO lists NAFDAC's Quality Control Laboratory in Yaba as prequalified from October 2023. An IMDRF document also records that NAFDAC became an affiliate member of the International Medical Device Regulators Forum in March 2024. These are institutional developments during her tenure rather than evidence of sole personal causation.
Adeyeye signed a NAFDAC directive dated 29 November 2023 stating that bioequivalence data would become mandatory from January 2025 for specified drug-product dossier submissions. The directive reflects her role in the agency's regulation of pharmaceutical product evaluation and registration.
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