Fast-tracking generic submissions

Are you in need of a combined generic drug bioequivalence testing and submission service? In the fast-paced world of registering generic products, time is of the essence for running the bioequivalence (BE) study, performing the bioanalysis, and writing the marketing authorisation application dossier (eCTD).  Our specialized clinical trial unit, provided by Clinical Trial Consultants AB,… Fortsätt läsa Fast-tracking generic submissions