An end-to-end cloud-hosted electronic Regulatory Document Management Software (rDMS) Get a Quote / Request a Demo Overview Expertise Features Overview Freyr rDMS is an end-to-end electronic Regulatory Document Management System (rDMS/eDMS) 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 rDMS – an electronic Regulatory Document Management Software (eDMS / rDMS) is built ground-up, keeping specific nuances and expectations of Regulatory strategies and operational functions in mind. Our solution combines end-to-end set of features spanning the whole document lifecycle from inception and authoring up to submission and archiving of Regulatory documents. With the capability to efficiently handle enterprise-wide content and with the ease of integration with legacy systems, Freyr rDMS provides a robust 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 lifecycle 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 Advance admin functions to manage users and monitor ground-level activity Easy management of document mode, status, and version Freyr rDMS Features Cloud-hosted eDMS Focuses primarily on storage and archiving and document lifecycle management Includes powerful work flow for incorporating business processes into the management of the documents Targets at storing and presenting documents in their native format (not limited to MS-Office products but including many different information formats) Advanced security restricting the access at document/folder level Provides document statistics based on – checked-in, checked-out, review, publish, and approve modes Advanced folder creation, management, view, and search functionality Comprehensive dashboard providing folder and document overview One-stop doc center to view and manage user access Doc groups to easily manage various documents Advanced search functionality based on doc groups and document meta tags Bulk action capability on clinical trial documents To Know More about Freyr rDMS, an electronic Regulatory Document Management System, and to take a feature-specific comprehensive product tour Get a Quote / Request a Demo
