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- Invitation to contribute to the upcoming EU multi-stakeholder workshop on clinical trial methodology on 23 November 2023 in Amsterdam
- Information on transition from NemID to MitID Erhverv
- New criteria for the notification of medicines supply shortages
- EMA is introducing Multi-Factor Authentication (MFA) for the Clinical Trial Information System (CTIS) from 01 June 2023.
- Registration of QPPV and PSMF number for veterinary medicinal products
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