New Jersey, 28 Jan 2016 – Freyr bags a critical project for providing specialized regulatory submissions services to a US based, Medical Instrumentation & Biotech Company. Freyr will provide its comprehensive support to help the client move from Paper-based to an electronic submission format. Under the scope of this project, Freyr will manage regulatory approvals, while efficiently managing multiple eCTD formats, documents and dossiers throughout the submission lifecycle. Freyr will provide eCTD services to enhance the submission procedure by bridging the gap between the time and market and minimizing expenses.

Implementing its strategic solutions, Freyr will streamline the electronic Health Authority Submission management process to ensure error free, timely and quality submissions throughout the challenging Submission Lifecycle timelines. Freyr has assisted a number of companies with its faster and efficient eCTD services in diverse segments of pharmaceutical industry such as medical device manufacturers, life sciences and consumer healthcare companies.