Unlocking the Path for FDA Philippines Approval for Products & Plants Registration

Unlocking the Path for FDA Philippines: Approval for Products and Plants Registration

What is FDA Philippines? The Food and Drug Administration (FDA) of the Philippines, established under Republic Act No. 3720 and later amended by Republic Act No. 9711, is responsible for ensuring the safety, efficacy, and quality of health products. This includes regulating food, drugs, cosmetics, medical devices, vaccines, and other health-related products such as pesticides […]

PPB Kenya Registration: Essential Guidelines for Sites and Products

PPB Kenya Registration: Essential Guidelines for Sites and Products

Describe PPB Kenya The Pharmacy and Poisons Board of Kenya is referred to as PPB Kenya. It is the regulatory organization in Kenya that oversees the registration, management, and control of medical devices, pharmaceuticals, and healthcare providers. Before these goods may be sold and utilized in the nation, the PPB makes sure they fulfil acceptable […]

Navigating the EU GMP Certification & Product Approval Process

Navigating the EU GMP Certification and Product Approval Process

EU GMP: What is it? EU GMP is Good Manufacturing Practices, promulgated by European Medicines Agency (EMA). EU GMP is the guidelines that pharma manufacturers must meet in their medicine manufacturing process. What is EMA? EMA is European Medicines Agency, established in 1995. The head office is in Amsterdam, the Netherlands. EMA is an agency […]

DIGEMID’S Approval Process: A Guide for Manufacturers and Exporters

DIGEMID’S Approval Process: A Guide For Manufacturers And Exporters

Introductory DIGEMID, the General Directorate of Medicines, Supplies, and Drugs in Peru, is a vital regulatory authority established on April 18, 1990, under the Ministry of Health. Its primary mission is to ensure that the Peruvian population has access to safe, effective, and high-quality medicines and health products. This agency plays a crucial role in […]

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