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Document: Regulatory Perspectives on Herbal Medicinal Botanical Drug Product Development - Joint FDA-EMA Workshop: Event agenda-2026/7/29
2026-07-30查看详情 > -
Document: List of medicinal products under additional monitoring-2026/7/29
2026-07-30查看详情 > -
Page: List of medicines under additional monitoring-2026/7/29
2026-07-30查看详情 > -
Document: List of medicinal products under additional monitoring-2026/7/29
2026-07-30查看详情 > -
Document: List of European Union reference dates (EURD) and frequency of submission of periodic safety update reports (PSURs)-2026/7/29
2026-07-30查看详情 > -
Document: Draft guideline on veterinary good pharmacovigilance practices (VGVP) - Module: Pharmacovigilance systems, their quality management systems and pharmacovigilance system master files - Revision 1-2026/7/27
2026-07-28查看详情 > -
Page: Podcast: Inside EMA-2026/7/27
2026-07-28查看详情 > -
Document: European Medicines Agency’s data protection notice for meeting registration forms via Microsoft Forms-2026/7/24
2026-07-26查看详情 > -
Document: European Medicines Agency’s data protection notice for conducting surveys via Microsoft Forms-2026/7/24
2026-07-26查看详情 > -
Document: European Medicines Agency’s data protection notice for meeting registration forms via EUSurvey-2026/7/24
2026-07-26查看详情 >