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IDMP COMPLIANCE through Master Data Management Most organizations and processes have grown either organically or through acquisition in ways that create data silos.  Most of IT systems are built with different data models. They implement different ways of describing doses or units of measurement among product lines....

ISO IDMP Timelines and Iteration Both the European Medical Agency (EMA) and the Food and Drugs Administration (FDA) are in the process of implementing the standards developed by the International Organization for Standardization (ISO) for the identification of medicinal products (IDMP). Following a phased implementation process, pharmaceutical...

New Clinical Data Publication Policy The European Agency proactively publishes the clinical reports submitted under the centralized marketing authorization procedure for human medicines. The policy entered into force on 1 January 2015 and is currently being implemented. The philosophy of this new Clinical data publication policy is in contradiction...