📆 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: [email protected]
