10 Small Submissions
No more than 10 Documents per submission
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.
achieve compliance
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.
functional highlights
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
key features
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
