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