Regulatory Publishing, Submissions, eCTD, NeeS format

Freyr assists Life sciences organizations streamline entire Health Authority (HA) Submission Management Process, right from dossier development, submission planning, tracking, publishing and final submission to HA including Delivery Confirmation/Acknowledgement, to ensure error free, timely and quality submissions throughout the Submissions Lifecycle. Freyr supports electronic, paper, eCTD, NeeS submission formats.

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