What Does IMPD Stand For?

IMPD stands for Investigational Medicinal Product Dossier EU

The Investigational Medicinal Product Dossier (IMPD) EU is a comprehensive document required for the submission of clinical trial applications within the European Union. It provides essential information about the investigational medicinal product, including its quality, manufacture, and control, as well as relevant preclinical and clinical data. The IMPD ensures that the product complies with regulatory standards, facilitating the assessment of its safety and efficacy prior to human trials.