How pharma firms assess their readiness for IDMP (Identification of Medicinal Products) is important for meeting compliance requirements and ensuring they are prepared for the digital product ...
Even now, after a decade of run-up, pharma’s readiness to implement and harness ISO IDMP standards still varies wildly, as does companies’ relative maturity in supporting FAIR data principles, geared ...
The European Medicines Agency (EMA) has recently published the second version of its EU IDMP Implementation Guide, and it is a landmark regulation for software vendors and pharma companies alike. This ...
All indications are that the July 2016 deadline for transition from Europe's eXtended EudraVigilance Medicinal Product Dictionary (XEVMPD) to the new Identification of Medicinal Products (IDMP) is not ...
As proof-of-concept projects begin to highlight IDMP’s different real-world use cases, and illustrate the potential benefits, stakeholders must come together and give greater emphasis to patients in ...
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