FREE WEBINAR | Data Management

January 26, 2022

📆 10/02/2022 🕛 3:00- 4:00 p.m. (CET)

➡️ ISO IDMP – Next Steps in the transition to ISO IDMP

The EMA, National Competent Agencies and Marketing Authorization Holders must use ISO IDMP standards for the exchange and communication of information on medicinal products.

EMA has started the phased implementation of SPOR and ISO IDMP. This will impact many areas of the pharmaceutical regulatory environment, both in the EU and other regions.

➡️ Are you ready to be ISO IDMP compliant?  Is your strategy for transitioning to ISO IDMP in place?

☑️ Do not miss this webinar with ASPHALION experts  Lidia Canovas and Lourdes Martin to know more about:

  • ISO IDMP Guideline ( Comments, Clarifications and watch outs)
  • Current timelines and expectations
  • Transition into ISO IDMP
  • RIM Systems and ISO IDMP
  • Strategies towards ISO IDMP Implementation

📧 For further information you can contact us at: info@asphalion.com

 

 

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ISO-IDMP O EL CAMBIO DE PARADIGMA EN LA INDUSTRIA FARMACÉUTICA

La Agencia Europea del Medicamento (EMA) ha comenzado la implementación de los estándares desarrollados por la Organización Internacional de Normalización (ISO, del inglés International Organization for Standardization) para la identificación única de medicamentos (IDMP, del inglés Identification of Medicinal Products).

2nd eAF (DADI) Newsletter has been published on the EMA website!

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