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Notice To All Stakeholders

The National Agency for Food and Drug Administration and Control (NAFDAC) has drafted the Regulations below for your comment(s) and contribution. All Stakeholders have 60 calendar days to send in their contributions. Please send all comments to regulatoryaffairs@nafdac.gov.ng

Draft Regulations

DateRegulationComment Period
21st September, 2019Good Pharmacovigilance Regulations 2019 (Draft)21st September - 21st November, 2019
20th August, 2019Recall, Disposal and Handling of Substandard and Falsified Medicinal Products Regulations (Draft)20th August - 19th October, 2019
23rd July, 2019Good Distribution Practice Regulation (Draft)23rd July - 20th September, 2019
11th July, 2019Clinical Trial Regulations (Draft)11th July - 9th September, 2019
4th July, 2019Good Manufacturing Practice For Pharmaceutical Products Regulations (Draft)5th July - 2nd September, 2019
27th June, 2019Controlled Medicines Regulation (Draft)27th June - 25th August, 2019