THE LAGOS STATE WASTEWATER MANAGEMENT OFFICE (LSWMO), YESTERDAY, SEALED OFF SOME BUILDINGS/PROPERTIES ACROSS THE STATE OVER DIFFERENT ENVIRONMENTAL INFRACTIONS.(PHOTO). #PRESS RELEASE

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 The Lagos State Wastewater Management Office (LSWMO), yesterday, sealed off some buildings/properties across the state over different environmental infractions. They are; * A property on 34, Adeniji Adele, Lagos Island for deliberate discharge of raw sewage into the public drain causing offensive odour and sewage flowing in the community, constituting public nuisance, environmental pollution and endangering human life. * A block of Shops along Powerline Road, Meiran, Alimosho, for the illegal construction and operation of unsanitary toilet facility on a road setback without a permit, constituting public nuisance, environmental pollution and endangering human life. * A three-storey building at 38, Adeniji Adele Street, Lagos Island for deliberate discharge of raw sewage into the public drain. * A building at H29, House of Jesus Street, Langbasa, Ibeju-Lekki, Lagos, for the deliberate discharge of raw sewage into the public drains. Residents are urged to adopt proper wastewater mana...

NIGERIA’S NAFDAC NOW A MEMBER OF ICH. (PHOTO). #PRESS RELEASE


 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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