Clinical trial exemption for medical implants: what changes for manufacturers in 2026
Delegated Regulation (EU) 2026/1451 updates the list of class III implants and devices exempt from prior clinical invest...
9 Articles
Delegated Regulation (EU) 2026/1451 updates the list of class III implants and devices exempt from prior clinical invest...
Decision 67/2026 of the EEE Joint Committee updates technical and certification requirements for products marketed in No...
EEA Joint Committee Decision 78/2026 updates certification and testing requirements for Norway, Iceland and Liechtenstei...
The EU updates harmonized standards for 9 categories of medical devices. Manufacturers and importers must review their c...
The EU opens negotiations with South Korea to mutually recognize product certifications. Exporters of machinery, electro...
Decision 11/2026 of the EEE updates certification standards in Norway, Iceland and Liechtenstein. Manufacturers and impo...
Decision 17/2026 of the EEE updates technical standards and certification from February 6, 2026. Manufacturers and impor...
Decision 281/2025 of the EEE updates technical certification requirements from 5/12/2025. Manufacturers and importers mu...
The EU updates harmonized technical standards in April 2026. Manufacturers and marketers must review their certification...