| dc.contributor.author | Ethiopian Food and Drug Authority | |
| dc.date.accessioned | 2026-02-24T07:32:38Z | |
| dc.date.available | 2026-02-24T07:32:38Z | |
| dc.date.issued | June 2025 | |
| dc.identifier.uri | http://repository.iphce.org/xmlui/handle/123456789/5332 | |
| dc.description.abstract | The Government of Ethiopia has been actively working to strengthen the regulatory system at both the national and regional levels. Ensuring the comprehensive regulation of all aspects related to the safety, efficacy, and quality of pharmaceutical products is a key priority. Effective medicines regulation encompasses various critical activities, including the inspection of pharmaceutical facilities such as manufacturers. These inspections play a vital role in safeguarding public health by ensuring compliance with Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), Good Storage Practice (GSP) and Good dispensing practices other regulatory standards. | en_US |
| dc.language.iso | en_US | en_US |
| dc.subject | pharmaceutical facilities | en_US |
| dc.title | GMP inspection manual, edition no. 03 | en_US |
| dc.type | Manual | en_US |