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Document: Process for the electronic submission of medicinal product information - Chapter 3-2026/6/16
2026-06-17查看详情 > -
Document: Committee for Advanced Therapies (CAT) rules of procedure-2026/6/16
2026-06-17查看详情 > -
Page: Contacting EMA: post-authorisation-2026/6/15
2026-06-16查看详情 > -
Page: Notifying EMA of changes to contact persons (veterinary medicines)-2026/6/15
2026-06-16查看详情 > -
Document: IRIS guide for applicants - How to create, submit and manage IRIS applications, for industry and individual applicants-2026/6/15
2026-06-16查看详情 > -
Document: IRIS guide to registration and RPIs-2026/6/15
2026-06-16查看详情 > -
Document: Lonquex : EPAR - Public assessment report-2026/6/12
2026-06-15查看详情 > -
Document: Products Management Services (PMS) public API - Terms and conditions-2026/6/12
2026-06-15查看详情 > -
Document: Regulatory Perspectives on Herbal Medicinal Botanical Drug Product Development - Joint FDA-EMA Workshop: Event agenda-2026/6/12
2026-06-15查看详情 > -
Document: Product Management Service (PMS) - Implementation of International Organization for Standardization (ISO) standards for Identification of Medicinal Products (IDMP) in Europe: Registration requirements to public PMS API (beta release) - Chapter 1
2026-06-15查看详情 >