Better identification of medicinal products
The European Medicines Agency (EMA) is currently implementing the standards developed by the International Organization for Standardization (ISO) for the identification of medicinal products (IDMP). To help all interested stakeholders prepare for the new requirements linked to IDMP, the Agency is organising a webinar on Thursday 4 August 2016, from 09:30 to 12:30 (UK time).
Click on this link for more information.
