10 Small Submissions
No more than 10 Documents per submission
Life sciences is a highly regulated industry, full of sensitive information that is required to be maintained efficiently. Documents are the backbone of any life sciences segment since it establishes the quality of processes and assurance of safety. The growing volume of documents in organizations exponentially increases the demand to replace traditional and manual documentation practices to reduce time, effort, and errors. In such scenarios, the absence of a proper Document Management System (DMS) increases the chance of misplacing critical documents and tracking changes significantly.
The major challenges in managing multiple documents include the following:
A smart and secure electronic Document Management System(eDMS) can provide precision and control for complex product development. Documents from diverse functional areas can be accessed easily without extra work or duplication, thanks to comprehensive content and data repositories. A robust content repository can help handle the data from all functional areas, including the previously developed documentation.
An eDMS enables teams to collaborate and get an outlook on global Regulatory operations. Freyr rDMS, an end-to-end electronic Regulatory Document Management System (rDMS/eDMS), is exclusively designed to enable Regulatory groups and departments within a life sciences organization to effortlessly create, capture, manage, organize, connect, deliver, and archive Regulatory data and documents. The solution is built from the ground up, cognizant of Regulatory strategies and operational functions.
Reach out to Freyr experts to understand electronic document management system. Click here to go through our proven software – Freyr eDMS/rDMS. Request a demo.