An India based fast growing integrated pharmaceuticals company approached Freyr for Regulatory support in preparation of nonclinical overviews for established medicinal products. The client was facing challenges with the project, as there was no Standard Operating Procedures (SOPs) with the client.
Through this case study, decipher how Freyr managed to establish a streamlined process to ensure successful completion of 10 nonclinical overviews and nonclinical summaries.
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