A leading pharmaceutical company approached Freyr for Regulatory support with the preparation of Permitted Daily Exposure (PDE) for APIs used in manufacturing of various drug products. Since, there are different routes of preparation of drugs in one facility; the client was facing challenges in streamlining the report preparation process.
Through this case study, know how Freyr equipped the client to clear the MHRA audit without any obstacles and delivered 125 PDE reports on time.
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