Overview
The Life Sciences industry is built on innovation in terms of their constant search for new drugs, devices, and cures. Technology has become ubiquitous in driving not only scientific innovation but also in building, integrating, and managing platforms that support scientific innovation.
At Freyr, we understand global Regulatory requirements management and its impact on day-to-day Regulatory decisions in strategy, submission planning, preparation, and dossier creation.
Freyr Digital is a complete suite of next-generation software solutions covering the whole of the lifecycle including labeling and artwork. Our solutions are fully compliant, deployed, and operational at scale, streamlining the Regulatory Ecosystem.
Our Products
Submission Management
Advanced eCTD software for the entire document lifecycle – from submission creation and publishing through tracking and managing your workflow. Know More
Create, capture, manage, deliver, monitor, and archive Regulatory data with an end-to-end electronic document management system. Know More
Regulatory Information Management
Advanced RIM solution for product registrations, lifecycle management, and their marketing status check. Know More
Regulatory Intelligence
Largest global ingredients repository and Regulatory database to support digitization of formulation assessment and real-time intelligence. Know More
Lead the market with a centralized repository with global access to market intelligence. Know More
Labeling and Artwork Management
Simplify the complexity of artwork development to create opportunities for cost savings within each stage of the artwork management process. Know More
A robust platform to create, validate, store, and submit complex content structures aligning with the SPL’s (FDA) and the SPM’s (HC) standard control vocabularies and validation rules. Know More