EURD ID
- Guideline or reference source
- PMS Implementation of ISO standards for IDMP in Europe Chapter 2 version 2.0
- Definition
- When the medicinal product is part of a PSUR single assessment procedure in accordance with the European Union reference date dates and frequency of submission of periodic safety reports list (EURD list), the EURD ID shall be provided. The EURD ID shall be derived from the procedure number of the PSUR single assessment.
- Related Term
- European Union reference dates
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