WHIPPANY, N.J.--(BUSINESS WIRE)--Cadence Pharmaceuticals, Inc., is now positioned to send regulatory submissions through the U.S. Food and Drug Administration’s Electronic Submissions Gateway (ESG) by using eCTDXPress, ISI’s market-leading software product for managing and reviewing electronic submissions. Cadence is a biopharmaceutical company focused on in-licensing as well as on developing and commercializing proprietary product candidates principally for use in hospital settings. Cadence submitted its first New Drug Application in May 2009 for its investigational product candidate, intravenous acetaminophen.
