Freyr assists Life Sciences organizations to streamline the entire Regulatory Publishing and Submissions management process. The process initiates right from dossier development that includes Regulatory submission planning, tracking, publishing, and making the final submissions to Health Authorities (HAs) including delivery confirmation/acknowledgment.

As global HAs are accepting submissions in the 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 proven itself for on-time Regulatory publishing and submission services for all kinds of acceptable formats such as paper, electronic submissions, eCTD, and NeeS.

Apart from deploying experienced Regulatory personnel, Freyr offers industry-proven eCTD publishing and electronic submission software, Freyr SUBMIT PRO, to enable companies effectively meet all their specific and unique Regulatory publishing and submission requirements for quick reviews and faster approvals of their products such as drugs, biologics, and medical devices.


Publishing and Submissions Expertise

Global HA Mandates