vimarsana.com
Home
Live Updates
FDA Accepts REGEN-COV® (casirivimab and imdevimab) for
FDA Accepts REGEN-COV® (casirivimab and imdevimab) for
FDA Accepts REGEN-COV® (casirivimab and imdevimab) for Priority Review for Treatment and Prophylaxis of COVID-19
/PRNewswire/ -- Regeneron Pharmaceuticals, Inc. (NASDAQ: REGN) today announced that the U.S. Food and Drug Administration (FDA) has accepted for priority...
Related Keywords
Japan ,
United States ,
India ,
United Kingdom ,
Brazil ,
South Africa ,
Colombia ,
Canada ,
Switzerland ,
September Regeneron ,
Georged Yancopoulos ,
Tammy Allen ,
Regeneron Velocimmune ,
Vesna Tosic ,
Twitter ,
Human Service Office Of The ,
Regeneron Velocimmune Technology ,
Nasdaq ,
Teva Pharmaceutical Industries Ltd ,
Department Of Health ,
European Union ,
Pharmaceuticals Inc ,
Centers For Disease ,
Regeneron Pharmaceuticals Inc ,
Biomedical Advanced Research ,
Regeneron Genetics Center ,
Human Services ,
Us Department Of Health ,
Drug Administration ,
Development Authority ,
Exchange Commission ,
European Medicines Agency ,
National Infusion Center Association ,
Biologics License Application ,
Marketing Authorization Application ,
Emergency Use Authorization ,
National Infusion Center ,
Human Service Office ,
Assistant Secretary ,
Fact Sheet ,
Chief Scientific Officer George ,
Authorized Use ,
Exposure Prophylaxis ,
Disease Control ,
Post Exposure Prophylaxis ,
Healthcare Providers ,
Dear Healthcare Provider Letter ,
Patient Fact ,
Identifying High Risk ,
Antiviral Resistance ,
Including Anaphylaxis ,
Infusion Related Reactions ,
Subcutaneous Dosing ,
Monitoring Recommendations ,
Specific Populations ,
Looking Statements ,
Regeneron Pharmaceuticals ,
Product Candidates ,
Biologics License Applications ,
Marketing Authorization Applications ,
Teva Pharmaceutical Industries ,
Nc ,