18 January 2023 The European Commission proposes an extension of the transitional period for the re-certification of medical devices
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