Freyr rDMS enables Regulatory teams to effortlessly create, capture, manage, organize, connect, deliver and archive Regulatory data and documents. We have built the solution from the ground-up keeping Regulatory strategies and operational functions in mind.
through light weight, yet powerful document management software
Designed especially for Regulatory teams in the Life Sciences organizations, Freyr rDMS provides end-to-end electronic document management (rDMS/eDMS). It can effortlessly create, capture, manage, deliver and archive Regulatory data and documents in a compliant, efficient and intuitive manner.
Freyr rDMS also has the capacity to handle enterprise-wide documentation and can easily be incorporated with legacy systems, providing a strong platform for knowledge sharing across the organization. This places your Regulatory function at the heart of your business, promoting compliance and reducing risk throughout your R&D life cycle.
parallel review - multiple user access to review and update documents
role-based and version-controlled documents
user specific document related notifications
ease of integration with legacy systems – internal and third-party
multiple deployment choices – private, public, hybrid, on-premises and cloud
intuitive and holistic dashboards and reports
seamless document monitoring
advanced admin functions to manage users and monitor ground-level activity
integrating multiple language resource files
seamless third-party integration
Migration-friendly and equipped with API and rest full services
intuitive user experience and simplified product usability