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SIFI ANNOUNCES EMA VALIDATION OF ITS MARKETING AUTHORISATION APPLICATION FOR AKANTIOR® FOR THE TREATMENT OF ACANTHAMOEBA KERATITIS AND THE OPENING OF AN EARLY ACCESS PROGRAM

SIFI ANNOUNCES EMA VALIDATION OF ITS MARKETING AUTHORISATION APPLICATION FOR AKANTIOR® FOR THE TREATMENT OF ACANTHAMOEBA KERATITIS AND THE OPENING OF AN EARLY ACCESS PROGRAM
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United Kingdom , John Dart , Dan Piggott , Manuela Marrano , University College London , Regulatory Affairs , European Commission , Early Access Program , Uniphar Group Product Access Division , Vincenzo Papahead Of Scientific Affairs , Institute Of Ophthalmology , European Medicines Agency , Healthcare Products Regulatory Agency , Polihexanide Access Program , Committee For Medicinal Products Human Use , Marketing Authorization Application , Honorary Clinical , Market Access , Medicinal Products , Human Use , Orphan Drug Designation , Uniphar Group , Product Access Division , Polihexanide Access , Managing Director , Product Access ,

SIFI RECEIVES FAVORABLE FEEDBACK FROM THE US FDA ON AKANTIOR® FOR THE TREATMENT OF ACANTHAMOEBA KERATITIS

SIFI RECEIVES FAVORABLE FEEDBACK FROM THE US FDA ON AKANTIOR® FOR THE TREATMENT OF ACANTHAMOEBA KERATITIS
streetinsider.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from streetinsider.com Daily Mail and Mail on Sunday newspapers.

United States , Manuela Marrano , Elmer Tu , Regulatory Affairs , Cornea Service , University Of Illinois Eye , University Of Iowa Hospitals Clinics Mr , Drug Administration , Orphan Drug Designation , United States Food , New Drug Application , Market Access , Clinical Ophthalmology , Illinois Eye , American Journal , Ophthalmology Case Reports , Iowa Hospitals , New Chemical Entity , Kleijnglobal Head ,

SIFI S.p.A.: SIFI RECEIVES FAVORABLE FEEDBACK FROM THE US FDA ON AKANTIOR FOR THE TREATMENT OF ACANTHAMOEBA KERATITIS

Type B meeting feedback confirms SIFI's view that no additional data will be required for potential FDA approval of AKANTIORAKANTIOR is poised to become the first FDA-approved medication for ....

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