In December of this year, the second version of the EU IDMP Implementation Guide is expected to be published and will contain updates on the Medicinal Product Information data model and the process of how product data is to be submitted as part of the TOM. This publication will be the start of a 24 month period before IDMP becomes mandatory for the industry as a whole.
Siniša Belina, Senior Life Sciences Consultant at Amplexor, will address the impact of the EU IDMP Implementation Guide on the Amplexor Life Sciences Suite by demonstrating the implementation of the required IDMP data fields as part of the ProductExpert solution. He will additionally discuss what processes need to be put in place to ensure compliance with the TOM within the RIMExpert solution.
This webinar will also feature Frits Stulp, Managing Director of Iperion Life Sciences Consultancy and IDMP expert, who will give a general status update on IDMP and will also cover data model updates, as well as the future data submission process according to the proposed TOM. This will also include some insights on how the current 3rd acknowledgment process will be addressed.