A U.S. based leading new drug development company was looking to partner with a Regulatory expert for assistance with the preparation of nonclinical overview text and nonclinical summaries as per module 2.4 and 2.6. Freyr assisted the client by accelerating the process and providing support in the nonclinical space within specified time.
Read the case study to know Freyr’s approach of handling the bottlenecks of the project and providing significant cost advantages.
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