What Does EDMF Stand For?

EDMF stands for European Drug Master File

EDMF, or European Drug Master File, is a comprehensive document that provides detailed information about the manufacturing, quality control, and specifications of a pharmaceutical product. It is submitted to regulatory authorities in Europe to support drug registration and ensure adherence to safety and efficacy standards. The EDMF is an integral part of the pharmaceutical regulatory framework, facilitating transparency and collaboration between manufacturers and health authorities.