idmp_activity_update_vada_perkins-openmedicine.pptVIP

FDA Implemented (IDMP/SPL) * Global Identification of Medicinal Products (IDMP) Lifecycle SPOR product and substance data submission: EMA will convert existing?medicinal product and substance entities into the new HL7 format and assist industry in the submission of IDMP products via the new format. Pharmaceutical companies will be required to confirm this conversion performed by EMA, and to enrich the data with additional information. XEVPRM format will then be decommissioned and the new format will become mandatory to comply with Article 57 data submission requirements. * MD5 message-dig