Frits Stulp, Managing Director, Iperion Life Sciences Consultancy / Siniša Belina, Amplexor's Senior Life Sciences Consultant
The second version of the EU IDMP Implementation Guide is expected to be published in December this year. This new release contains updates on the Medicinal Product Information data model and the process of how the product data should be submitted as part of the Target Operating Model (TOM). This publication will be the start of the 24-month period before IDMP becomes mandatory for the industry.
In this webinar Frits Stulp, Managing Director of Iperion Life Sciences Consultancy and IDMP expert will give a general status update on IDMP. He will cover data model updates as well as the future data submission process according to the proposed TOM, including insights on how the current 3rd acknowledgement process will be addressed.
Siniša Belina, Amplexor's Senior Life Sciences Consultant, will present the impact of the EU IDMP Implementation Guide on the AMPLEXOR Life Sciences Suite. He will demonstrate the implementation of the required IDMP data fields as part of the ProductExpert solution as well as discuss what processes need to be in place to comply with the TOM within the RIMExpert solution.