IMPD
This glossary item is used in the courses Clinical Research in the Netherlands - Legislation & Procedures & Market Approval Online
IMPD
Investigational Medicinal Product Dossier, document to obtain clinical trial approval for a medicinal product (EU terminology; IND for US); named Investigational Medical Device Dossier (IMDD) for medical devices.
Investigational Medicinal Product Dossier
Clinical Research in the Netherlands - Legislation & Procedures
Before starting a medical research study, it is reviewed and approved by an authorized reviewing committee. Learn the practical steps to navigate the review system of clinical research. This course is specific for the Netherlands.
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Market Approval Online
Market Approval is mandatory at various milestones in the development of your novel biomedical intervention and need to be passed to move your product to the market and beyond.