Freyr assists Life Sciences organizations to streamline entire Regulatory submissions management process, right from dossier development, submission planning, tracking, publishing and final submissions to Health Authorities (HAs) including delivery confirmation/acknowledgement.

As global HAs are accepting submissions in electronic format, the need of the hour is to deploy robust and ever-updated publishing and submission tools to manage region-wise submissions and region-specific formats. Freyr ensures error-free Regulatory submissions with utmost quality and has been proven for on-time Regulatory publishing and submission services for all kinds of submission formats such as: paper, electronic, eCTD, and NeeS.

Apart from deploying experienced Regulatory personnel, Freyr offers industry-proven eCTD publishing and submission software, Freyr SUBMIT PRO, to enable companies effectively meet all their specific and unique Regulatory submission requirements for quick reviews and faster approvals of their products; Drugs, Biologics, and Medical Devices.