Regulatory News

BIOMERIEUX (EPA:BIM)
13/10/2023 07:02
bioMérieux announces CE-marking of VIDAS® TBI (GFAP, UCH-L1), a test for improved assessment of patients with mild traumatic brain injury, including concussion
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BIOMERIEUX (EPA:BIM)
22/09/2023 07:01
bioMérieux submits Dual 510(k) and CLIA-waiver application to FDA for the BIOFIRE® SPOTFIRE® Respiratory/Sore Throat (R/ST) Panel
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BIOMERIEUX (EPA:BIM)
01/09/2023 07:01
bioMérieux – First-Half 2023 Results
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BIOMERIEUX (EPA:BIM)
27/06/2023 18:31
bioMérieux’s Executive Committee evolves: Jennifer Zinn appointed Executive Vice President of Clinical Operations
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BIOMERIEUX (EPA:BIM)
14/06/2023 07:26
bioMérieux evolves its governance: Alexandre Mérieux becomes Executive Chairman. Pierre Boulud is appointed Chief Executive Officer
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BIOMERIEUX (EPA:BIM)
09/05/2023 18:05
bioMérieux receives US FDA CLIA-waiver for the BIOFIRE® SPOTFIRE® Respiratory (R) Panel Mini
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BIOMERIEUX (EPA:BIM)
27/04/2023 07:02
bioMérieux – First-Quarter 2023 Business Review
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BIOMERIEUX (EPA:BIM)
14/04/2023 18:01
Oxford Nanopore and bioMérieux to enter into a strategic partnership agreement to develop innovative infectious disease diagnostics
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BIOMERIEUX (EPA:BIM)
13/04/2023 18:31
bioMérieux receives US FDA 510(k) clearance for the BIOFIRE® SPOTFIRE® Respiratory (R) Panel Mini and will apply for CLIA-waiver
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BIOMERIEUX (EPA:BIM)
07/04/2023 07:01
SPECIFIC REVEAL™ Rapid AST System, newly renamed VITEK® REVEAL™, submitted to US FDA for 510(k) clearance
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