‎‎NAF RECEIVES FIVE NEW HELICOPTERS AS FG ACCELERATES AIRPOWER MODERNISATION. (PHOTO).

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 ‎‎NAF RECEIVES FIVE NEW HELICOPTERS AS FG ACCELERATES AIRPOWER MODERNISATION ‎ The Nigerian Air Force (NAF) has taken delivery of five new helicopters as the Federal Government accelerates efforts to modernize Nigeria’s airpower capabilities and strengthen the Armed Forces’ capacity to respond effectively to contemporary security challenges.  ‎ ‎A statement by the Director of Public Relations and Information Air Commodore Ehimen Ejodame indicates that the platforms comprise three AW-109 Trekker B helicopters  and two H-125 helicopters. ‎ The three AW-109s, which form part of 10 recently acquired by the Federal Government, were received in Lagos on 15 September 2026, with the remaining seven expected to be delivered before the end of 2026. ‎ ‎The Chief of the Air Staff, Air Marshal Sunday Aneke, described the acquisition as another significant milestone in the Federal Government’s sustained investment in the modernization and re-equipment of the NAF noting that the new pl...
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NIGERIA’S NAFDAC NOW A MEMBER OF ICH. (PHOTO). #PRESS RELEASE

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 Nigeria’s NAFDAC now a member of ICH


The International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) has confirmed Nigeria as a member.

Nigeria’s NAFDAC was admitted when the ICH Assembly met in Singapore from 18 to 19 November 2025, during its second in-person meeting this year. 


At the same assembly, South Africa’s SAHPRA was also admitted as a member, while DIGEMAPS, the Dominican Republic, and the Philippine FDA were admitted as Observers.


The 35-year-old ICH now has 25 Members and 41 Observers. 


ICH Membership criteria for national regulatory authorities include implementation of at least the three Tier 1 ICH Guidelines (Q1 Stability Testing Guidelines, Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients, and E6 Good Clinical Practice Guideline), participation in ICH biannual meetings, and a plan for implementing all ICH Guidelines. 


ICH brings together regulatory authorities and the pharmaceutical industry to discuss the scientific and technical aspects of pharmaceutical development. 


The association produces harmonised technical requirements to ensure the development and registration of safe, effective and high-quality medicines for human use.

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