Guidance on good manufacturing practice and good distribution practice: Questions and answers By EMA – Inspection
Confidentiality arrangement between the EU and the Republic of Korea By EMA – News and press releases
Guidance on the anonymisation of protected personal data and assessment of commercially confidential information during the preparation of RMPs (main body and annexes 4 and 6) By EMA – Regulatory and procedural guidelines
Meeting highlights from the Committee for Medicinal Products for Human Use (CHMP) 22-25 April 2024 By EMA – News and press releases
Follow up EMA and EORTC multi-stakeholder workshop on soft tissue and bone sarcoma, Online, European Medicines Agency, Amsterdam, the Netherlands, 24 May 2024 By EMA – Events
EMA workshop on the challenges in drug development, regulation and clinical practice in hemoglobinopathies, Online, European Medicines Agency, Amsterdam, the Netherlands, from 1 July 2024, 14:00 (CEST) to 1 July 2024, 18:00 (CEST) By EMA – Events