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Document: Procedural advice for orphan medicinal product designation: Guidance for sponsors-2026/4/16
2026-04-17查看详情 > -
Document: Chapter 3.II: XEVPRM detailed user guidance on the electronic submission of information on medicinal products for human use by marketing authorisation holders to the EMA-2026/4/16
2026-04-17查看详情 > -
Document: Regulatory Procedure Management in IRIS roadmap-2026/4/16
2026-04-17查看详情 > -
Page: CHMP opinions on consultation procedures on ancillary substances incorporated in a medical device-2026/4/16
2026-04-17查看详情 > -
Document: IVF Media G5 - Procedural steps and scientific information after initial consultation-2026/4/16
2026-04-17查看详情 > -
Document: Procedural advice on paediatric applications-2026/4/16
2026-04-17查看详情 > -
Document: Template for scientific document for paediatric investigation plan or product-specific waiver-2026/4/16
2026-04-17查看详情 > -
Document: Paediatric investigation plan (PIP) - Key elements form-2026/4/16
2026-04-17查看详情 > -
Page: EU Innovation Network (EU-IN)-2026/4/15
2026-04-16查看详情 > -
Document: Radiopharmaceuticals EU-IN Horizon Scanning Report-2026/4/15
2026-04-16查看详情 >