A U.S. based, manufacturer of OTC and Prescription Drug Products, the client was looking for review of raw data and compilation of affected sections including administrative documents and submission to the USFDA within a short span of time. Without a proper Regulatory expertise, the client was facing issues with the process.
Read the case to know how Freyr helped in providing timely review of the raw data as and when received from the client and performed the complete Gap Analysis.
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