rdms

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

Quick Inquiry
x