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What is the procedure if the medical device was supplied without telling the manufacturer? FAQ

In case of receiving inquiries from SFDA about a medical device Field Safety Corrective Action that they received from more than one source, but for the company is considered as one Field Safety Notice should all of them be closed, or it should be reported that they are the same Field Safety Notice which was previously answered? FAQ

Awareness Campaigns of Diseases and Health Education Regulations Regulations

Republic of Uganda Country

“SFDA” Warns Against Lip-Care Product due to Contain High Levels of Lead and Arsenic Warnings

Xarelto (Rivaroxaban) Risk Minimization Activity

Amlor plus (Amlodipine besylate valsartan) Risk Minimization Activity

Valtense Plus (Hydrochlorothiazide, Valsartan) Risk Minimization Activity

pazopanib Risk Minimization Activity

OFEV (nintedanib) Risk Minimization Activity