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This is a closed event. We already had presentation from a number of partners and this time we kindly invite: - BfARM (DE) - ARMPS (BE) - INFARMED (PT) to present lessons learnt from their view. We also invite ALL partners to share experiencies during the discussion. |
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The UNICOM Trans-Atlantic meeting will be officially coordinated by *CTADHL, a UNICOM partner formally tasked for trans-Atlantic outreach by UNICOM to include promotion and adoption of ISO IDMP across the medicinal product lifecycle. Although UNICOM is an EU initiative, it strongly considers collaboration and exchange with North American stakeholders as part of its remit to […] |
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Topic: Using IDMP in Adverse Event reporting and Individual Case Safety Reports (ICSR) Date: 3 December between 3 – 4:30 pm CET Presenters: Anja van Haren Barry Hammond (UNICOM WP 1 and MedDRA) Sarah Vaughn (MHRA) Panelists: Julie James (UNICOM WP 9 and BlueWaves) Jane Millar ( UNICOM WP 1 and SNOMED CT) |
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