Freyr assists Life Sciences organizations to streamline the entire Regulatory submissions management process. It includes dossier development, submission planning, tracking, publishing, and making final submissions to Health Authorities (HAs), in addition to delivery confirmation/acknowledgment.

As global HAs are accepting submissions in the electronic format, the need of the hour is to deploy robust and upgraded 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 as a prompt Regulatory publishing and submission services provider for all kinds of submission formats such as paper, electronic, electronic Common Technical Document (eCTD), and NeeS.

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