The client is a leading China-based biopharmaceutical company specializing in developing, producing, and commercializing drugs and medical devices. The client required a Regulatory document management tool with single and collaborative authoring and reviewing capabilities. Freyr assisted the client with the in-house cloud-hosted software - Freyr rDMS, which allows concurrent authoring, document management, seamless tracking of changes, and archives Regulatory data for submissions.
Download the proven case study to know how Freyr rDMS was integrated with the client’s platform that optimized document management.
