Freyr assists Life Sciences organizations to streamline entire Health Authority (HA) submission management process, right from dossier development, submission planning, tracking, publishing and final submissions to HA including delivery confirmation/acknowledgement, to ensure error free, timely and quality submissions throughout the submission lifecycle. With expertise in Regulatory publishing services, Freyr supports paper, electronic, eCTD, NeeS submission formats.

With a flexible publishing and submission software, Freyr SUBMIT, Freyr enables companies to effectively meet all their specific and unique Regulatory submission requirements for faster and efficient approval of Drugs, Biologics and Medical Devices by global HAs.