The case study showcases Freyr Digital’s serving as the virtual Regulatory Affairs Solutions Provider for a US-based generic pharmaceutical company. The key challenges addressed include managing end-to-end regulatory submissions and document management through a centralized repository, ensuring seamless access to documents for internal and external stakeholders, and efficient SPL creation and management.
Freyr Digital's solutions, including Freyr rDMS, Freyr SUBMIT PRO, and Freyr SPL-SPM, provided the client with streamlined submission processes, centralized document access, better oversight, and real-time insights, enhancing efficiency, reducing costs, and improving turnaround times (TAT).
Discover how Freyr Digital successfully reduced submission preparation time by 30%, achieved 100% regulatory compliance, and improved document processing efficiency by 40%, all while cutting review cycles by 25%.
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