Regulatory Document Management System (RDMS) Services

Freyr rDMS is an end-to-end electronic Regulatory Document Management system exclusively designed to enable Regulatory Groups and Departments within a life sciences organization to seamlessly create, capture, manage, organize, connect, deliver and archive regulatory data and documents in a compliant, efficient and intuitive manner.
While traditional Document Management Software Solutions are typically retrofit for regulatory needs, Freyr Regulatory Document Management Software is built ground-up, keeping specific nuances and expectations of regulatory strategies and operation functions in mind. Our solution combines an end-to-end set of features spanning the whole document lifecycle from inception and authoring up to submission and archiving of regulatory documents.
With capabilities to efficiently handle enterprise-wide content and ease of integration with legacy systems, Freyr rDMS provides an integrated platform to address the critical need for knowledge sharing across the enterprise.

Regulatory Document Management System (RDMS)

Comments

Popular posts from this blog

Medical Device Regulation Report, Morocco, Registration

Medical Device Registration in Germany, IVDs, CE marking, EU MDR

Health Authority Queries – Responses | Interactions