As part of its surveillance activities, the FDA has recently noted an emerging trend in the poor handling of the key ingredients used in the preparation of one of Ghana's local delicacies called "Tuo Zaafi" which requires prompt actions from all..
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This year, the Ministry of Health in collaboration with Food and Drugs Authority (FDA), World Health Organization, Ghana Health Service, Vision for Alternative Development (VALD) and other Civil Society Organisations join in with the focus on growing sustainable food cr.
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The Food and Drugs Authority (FDA) is alerting healthcare professionals and the public about a recent incident of contamination of two batches of Norvasc 5mg tablets (FR3135 and FT2343) produced by the American Pharmaceutical Company, Viatris Inc..
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This is to remind you that in line with Section 112(e) of the Fourth Schedule of the Public Health Act, 2012 (ACT 851) and the recommendation of the Food and Drugs Authority's Technical Advisory Committee on Nutrition, The FDA has started full implementation of the Prov.
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During its routine market surveillance activities, the Food and Drugs Authority (FDA) has detected the presence of unregistered OXYTOCIN INJECTION 10iu/ml in some health facilities, including pharmacies in the country..
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COMMUNICATION OF UPDATED GUIDANCE
PROPER PLATFORM FOR ELECTRONIC REGULATORY COMPLIANCE - PHASE/LEVEL 2.
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The Food and Drugs Authority (FDA) is alerting the public about a recent major incidence of contamination of two brands of eyedrops, EZRICARE ARTIFICIAL TEARS and DELSAM PHARMA'S ARTIFICIAL TEARS owned by Global Pharma. Global Pharma has since issued a voluntary recall .
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SUSPECTED FALSIFIED ANTIMALARIAL DRUG ON THE GHANAIAN MARKET.
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The FDA exist to ensure the safety, quality and efficacy of human and veterinary drugs, food, biological products, cosmetics, medical devices, household chemical substances and clinical trials, and the control of tobacco products through the enforcement of relevant standards to protect public health.