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BioWorld - Sunday, March 22, 2026
Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Feb. 27, 2017

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EU finalizes more stringent CE mark rules with explosive 'supernova' of regulation

PARIS – The CE mark is dead, long live the new CE mark. Five years after launching a reform of regulations for commercializing medical devices and in vitro diagnostics (IVDs), the European Council released the final text for the Medical Device Regulations (MDR) and IVD Regulations (IVDR), setting in motion a countdown to enforcement. Read More

Advisory panel sees a place for Claret's Sentinel in cath lab

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Siemens' Digital Ecosystem combines imaging, diagnostic and medical data

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Intersect Ent picks up FDA nod for sinus treatment implant

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U.S. Supreme Court reverses Federal Circuit in Promega patent spat with Life Technologies

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