IDMP and SPOR: EMA Plans Published

One of the biggest concerns about implementation of IDMP in Europe has been that the plans were vague, and slipped frequently. European Medicines Agency (EMA) has just published a presentation with a detailed roadmap for the SPOR project and IDMP. The IRISS Forum also posted a summary of recent activity, but it’s limited to IRISS …

ARIM Registrations, EMA, IDMP, XEVMPD

XEVMPD: Unpacking its impact on IDMP

Note: This article is not a commitment to features or capabilities of ACUTA products or services. When ACUTA added the Registration module to to ARIM version 3.0 in 2017, our expectation was that IDMP (Identification of Medicinal Products, the ISO standards being implemented first in Europe) was imminent. Because of that, we expected it would …


Would you support IDMP that isn’t IDMP?

Joel Finkle, Director Regulatory Innovation & IDMP Strategy For the last few months – both at the January and March EU IDMP/SPOR Task Force Meetings, there has been debate about how to send IDMP data to agencies in Europe. Although the ISO standard specifies the HL7 SPL format, the initial iteration of EMA’s implementation is …