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Guidelines for Medical Devices GMP Inspection

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Guidelines for Medical Devices GMP Inspection

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To protect and promote public health by ensuring the safety, effectiveness, quality and proper use of regulated products through licensing, inspection, registration, laboratory testing, post-marketing surveillance, community participation, and provision of up-to-date regulatory information.

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Recent News

The Authority Begins Quality Testing of Drug Samples for African Countries
November 15, 2024
Ethiopian Food and Drug Authority Inaugurates New Day-care Centre
October 21, 2024
EFDA, AHRI, and USP/PQM Plus Collaborate with Local Pharmaceutical Manufacturers to Implement National Bioequivalence Roadmap
October 21, 2024

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