The client was a USA-based leading pharmaceutical company looking for support in IND submissions and amendments in existing documents. The project presented with end-to-end publishing activities which had to be completed in a short period. Freyr offered granular document level publishing services, including the review of source documents, and was able to make the IND submissions and document amendments on time. With zero errors and no warnings from the CDSCO, Freyr made it a successful collaboration in every aspect.
Learn how Freyr was able to offer comprehensive Regulatory services to the client by making high-quality submissions in the specified time with industry-approved tools. Download the proven case.
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