The client is a Greece-based pharmaceutical company focused on manufacturing and marketing health care products. The client was looking for a Software Solution that could compile, validate, publish, track and manage the dossiers for eCTD and NEES submissions for their Generic product portfolio. Freyr assisted the client by providing end-to-end eCTD solution software to meet the eCTD publishing and submissions commitments within stipulated timelines.

Find out how Freyr provided end-to-end Regulatory compliance support for eCTD publishing and submissions within the specified deadlines. Download the case study.