WHO-GMP (World Health Organization - Good Manufacturing Practices

The National Drug Authority (NDA) is the government agency responsible for regulating pharmaceuticals and healthcare products in Uganda

The Pharmacy and Poisons Board (PPB) is the National Medicines Regulatory Authority of Kenya

TFDA (Tanzania Food and Drugs Authority) has been renamed to the Tanzania Medicines and Medical Devices Authority (TMDA)

The Ethiopian Food and Drug Authority (EFDA) is the national regulatory body responsible for ensuring the safety, quality, and efficacy of food, medicines, medical devices, cosmetics, and other health-related products in Ethiopia

The Saudi Food and Drug Authority (SFDA) is the primary government body responsible for ensuring the safety, quality, and efficacy of food, drugs, and medical devices in Saudi Arabia

The Ministry of Health of the Republic of Uzbekistan (MOH) is the central government body responsible for managing healthcare, medical services, and pharmaceutical regulation across the country

EU GMP (European Union Good Manufacturing Practice) refers to the regulatory framework that ensures pharmaceutical products are consistently produced and controlled according to high-quality standards