Bio News
DIO has received European Medical Device Regulation (MDR) certification for its next-generation products, SICON and Prism X. Following the certification of UNICON, launched last year, the approval provides a regulatory basis for the two products to enter the European market.
Prism X will be unveiled for the first time at the DIO International Meeting, held Oct. 10-11 at COEX.
Biobook Team
biobookmedia@biobook.co.krRoche’s New Drug for Uveitic Macular Edema Faces FDA Decision in July 2027
BMS Reports Concurrent Phase 3 Success in Idiopathic Pulmonary Fibrosis and Solid Tumors
Merck’s $1.3 trillion eye disease drug raises safety and efficacy concerns: “Limited competitiveness”
CHA Biotech Holds 24.23% Stake in CMG Pharmaceutical as Share Consolidation Reduces Its Share Count
Rural Development Administration Develops Two Molecular Markers to Identify Leaf Splitting in Squash
MFDS Begins Distribution of Internationally Certified Reference Materials, Including 24 New Items, for a Total of 882
