Regulatory Document Management system, electronic rDMS

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.

Freyr rDMS Expertise

• End-to-end set of features spanning the whole document life cycle from inception and authoring up to submission and archiving of Regulatory documents

• Seamless organization of document monitoring process to ensure compliance with worldwide Regulatory authorities

• Robust and secure tools to manage an extensive range of Regulatory documents associated with business extents controlled by the Food and Drug Administration (FDA) and other international Regulatory systems

• Advanced admin functions to manage users and monitor activity

• Easy management of document mode, status, and version